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Recalls affecting Colorado

Data last updated: September 7, 2026 at 2:36 PM UTC

16,626 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Men — dietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

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Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 4, 2026

Foods Alive — Moringa Leaf Powder

Potential to be contaminated with Salmonella

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Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun — 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

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Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 3, 2026

Great Value — Organic Triple Berry Blend

Possible E. Coli Contamination

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Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc. — Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

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Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

Lipofit — Lipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

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Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

Kofinas — Garlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

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Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenUndeclaredAnnounced August 31, 2026

Little Temptations — Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

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Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Everything Sprouts — Robust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

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Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Martina — Mangoes

Potential contamination with Salmonella

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Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
NewestOldest
High riskLow riskAll
Wording
Class IIModerate risk
FoodAllergenUndeclaredRecalled February 1, 2016

Lysander's All Natural Bourbon Flavor Rub; for beef, chicken, pork, and fish; 3.8 oz (107.7 g), foil bag, 6 units per case. Manufactured by Geneva Foods, LLC.

Product contains not listed on the label allergens soy and wheat. Also does not declare sulfites.

ALL 50 STATES
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A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2081-2016
Lot/product code:
Lot codes ending in 14 or 15; UPC: 0-34795-00049-5.
Recalling firm:
Geneva Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenUndeclaredRecalled February 1, 2016

Lysander's All Natural Spicy Bourbon Flavor Rub; for beef, chicken, pork, and fish; 3.8 oz (107.7 g) foil bag, 6 units per case. Manufactured by Geneva Foods, LLC.

Product contains not listed on the label allergens soy and wheat. Also does not declare sulfites.

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2080-2016
Lot/product code:
Lot codes ending in 14 or 15; UPC: 0-34795-00051-8
Recalling firm:
Geneva Foods, LLC
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled February 2, 2016

Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection Type 1, USP, 1000 mL Single-Dose Container bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7965-09, Barcode (01) 0 030409 796509 0.

Labeling: Incorrect or Missing Lot and/or Exp Date: Confirmed customer report of an incorrect expiration date printed on the primary container labeled "01AUG1017" rather than "01AUG2017".

ALL 50 STATES
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A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0727-2016
Lot/product code:
Lot #: 56-853-FW, Exp 01AUG2017
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 19, 2016

Apollo EZ: Model: 9784152036 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.

The analysis showed that the incident was caused by a chain of four faults: 1.) The injured person overcame a physical barrier (the tabletop support arm. height ca. 60 em) to access a prohibited area not intended as a working position. 2) The directions for use (device labeling and instructions for use) did not contain an explicit exclusion of the prohibited area. 3.) The movement was activated inadvertently and continuously. and it was not released (the movement requires continuous activation). 4.) Delayed activation of the emergency stop.

ALAZCACOCTDCFLIAILINLAMAMDMIMNMOMSNJNYOHPAPRTNTXUTWI
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
73459
Lot/product code:
13101261
Recalling firm:
Villa Radiology Systems LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 19, 2016

Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.

The analysis showed that the incident was caused by a chain of four faults: 1.) The injured person overcame a physical barrier (the tabletop support arm. height ca. 60 em) to access a prohibited area not intended as a working position. 2) The directions for use (device labeling and instructions for use) did not contain an explicit exclusion of the prohibited area. 3.) The movement was activated inadvertently and continuously. and it was not released (the movement requires continuous activation). 4.) Delayed activation of the emergency stop.

ALAZCACOCTDCFLIAILINLAMAMDMIMNMOMSNJNYOHPAPRTNTXUTWI
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
73459
Lot/product code:
10110770 11030805 11030806 11070845 11070848 11070849 11090864 11110900 12020978 12020982 12030999 12041003 12061014 12061018 12061020 12081040 12091074 12101104 12121186 12121187 13031215 13101263 14021301 14031313 14041321 14051332 14071353 14081359 14091368 14091371 14121400 14121403 15021426 15031440 15041444 15091473 15091478 15101484 15101487
Recalling firm:
Villa Radiology Systems LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 19, 2016

Apollo: Models: 9784000131, 9784000231, 9784020131, 9784020231, 9784100231, 9784120131, 9784120231, 9784130131 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.

The analysis showed that the incident was caused by a chain of four faults: 1.) The injured person overcame a physical barrier (the tabletop support arm. height ca. 60 em) to access a prohibited area not intended as a working position. 2) The directions for use (device labeling and instructions for use) did not contain an explicit exclusion of the prohibited area. 3.) The movement was activated inadvertently and continuously. and it was not released (the movement requires continuous activation). 4.) Delayed activation of the emergency stop.

ALAZCACOCTDCFLIAILINLAMAMDMIMNMOMSNJNYOHPAPRTNTXUTWI
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
73459
Lot/product code:
06040078 07030172 06090116 06110138 07010149 07020158 07020162 07020163 07020165 07030168 07030171 07040206 09090605 10100752 06060086 06100127 09010566 08020473 11100873 15041446
Recalling firm:
Villa Radiology Systems LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 19, 2016

Apollo DRF: Model: 9784220831 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.

The analysis showed that the incident was caused by a chain of four faults: 1.) The injured person overcame a physical barrier (the tabletop support arm. height ca. 60 em) to access a prohibited area not intended as a working position. 2) The directions for use (device labeling and instructions for use) did not contain an explicit exclusion of the prohibited area. 3.) The movement was activated inadvertently and continuously. and it was not released (the movement requires continuous activation). 4.) Delayed activation of the emergency stop.

ALAZCACOCTDCFLIAILINLAMAMDMIMNMOMSNJNYOHPAPRTNTXUTWI
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
73459
Lot/product code:
08090531 09090591 10040680 15051450 11020798
Recalling firm:
Villa Radiology Systems LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 29, 2016

Medica ISE Module Calibrant A; 500 mL - 140 mmol/L Na+, 125 mmol/L Cl-, buffers and preservatives; For use with ISE Module; Product Usage: Calibrations of ISE Model for integrated electrolyte system analysis.

Lot was not functioning properly and not exhibiting the correct physical properties.

ALL 50 STATES
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FDA has not published a risk classification for this recall yet.

Recall #:
77481
Lot/product code:
P/N 5409; Lot No. 15251; Exp. Date 09/2016
Recalling firm:
AMS Diagnostics, LLC
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled March 15, 2016

Quelicin (Succinylcholine Chloride) Injection, USP 200 mg. (20 mg/mL), 10 mL Multiple-dose vial, packaged in 25 Unit vials per carton, Rx only, HOSPIRA, INC., LAKE FOREST, IL 60045 USA, NDC 0409-6629-02

Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for the lot number and/or expiration date to be faded or missing from the primary label on the glass vial.

ALL 50 STATES
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A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0836-2016
Lot/product code:
Lot 52-045-EV, Exp 07/1/2016
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 18, 2016

8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL), 4.2 grams (84 mg/mL), 50 mL, Rx only, Hospira Inc, Lake Forest, IL 60045, NDC 0409-6625-02

Presence of Particulate Matter: particulate matter identified as an insect in one vial.

ALL 50 STATES
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The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0865-2016
Lot/product code:
Lot # 56-148-EV, Exp 8/1/2017
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 23, 2016

Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2168-02, barcode (01) 2 030409 216802 5.

Presence of Particulate Matter: Confirmed customer complaint for the presence of particulate matter.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-1137-2016
Lot/product code:
Lot #: 50-343-DK*, Exp 01FEB2017; note that the lot number may be followed by numbers from 01 to 99.
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled March 23, 2016

Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2168-02, barcode (01) 2 030409 216802 5.

Failed pH Specifications: Confirmed high not meeting quality requirements (OOS) results for pH.

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A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0854-2016
Lot/product code:
Lot #: 42-335-DK, Exp 1JUN2016; 48-128-DK, 48-129-DK, 48-261-DK, 48-262-DK, 48-351-DK, Exp 1DEC2016; 52-361-DK, Exp 1APR2017; note that the lot number may be followed by numbers from 01 to 99.
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled March 31, 2016

LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL

Marketed Without An Approved NDA/ANDA: Contains an unapproved drug, ligandrol LGD-4033

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A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0910-2016
Lot/product code:
Lot # 21511166, Exp 11/18
Recalling firm:
Invisiblu International LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled April 2, 2016

Human Chorionic Gonadotropin, 15,000 IU per vial, lyophilized for injection, Rx only, Complete Pharmacy & Medical Solutions, Miami Lakes, FL 33014

Non-sterility - presence of bacteria confirmed by outside laboratory after day 14.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0918-2017
Lot/product code:
Lot # 22016, Exp 1/30/2017
Recalling firm:
Complete Pharmacy and Medical Solutions LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 11, 2016

TRUE 3D VIEWER SYSTEM Model Number EP-00001-XX Software versions 1.0, 1.25, and 1.35 The t3D-Viewer is designed for use by health care professionals HCPs and is intended to assist the clinician who is responsible for making all patient management decisions. The True 3D Viewer (t3D-Viewer) system is comprised of a commercial off the shelf hardware platform and a proprietary software application that enables a health care professional (HCP) to visualize and interact with CT and MRI DICOM image data to assist in clinical decision making. The t3D-Viewer system hardware platform is comprised of an off the shelf stereoscopic display, an optical or electromagnetic motion tracking system and a computer system.

Imaging system data may be displayed with an incorrect orientation (sidedness) where the patient side is not correct (left, right, superior, inferior, anterior or posterior). This may lead to an inaccurate measurements.

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FDA has not published a risk classification for this recall yet.

Recall #:
96629
Lot/product code:
Model Number EP-00001-XX with software versions 1.0, 1.25, and 1.35 UDI-DI Codes: 00851325007003 Serial Numbers: Field Products: C2015-09-0001 C2015-09-0003 D2015-05-0002 C2015-06-0002 D2015-12-0004 C2015-08-0001 D2015-12-0005 C2015-09-0002 D2015-12-0001 C2016-01-0001 D2015-12-0002 C2015-12-0002 D2015-12-0003 D2016-01-0002
Recalling firm:
Echopixel, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2016

Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift

The design of the seats did not consistently have the adequate strength required to support the customers weight with continued use.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88610
Lot/product code:
Acorn 130/180 Seat Squab, included as part of The Acorn 130 Straight Stairlift and the Acorn 180 Curved Stairlift. Serial Numbers: 140110386215,140110356934,140110330295,140110410265,140110356903,140110319711,140110353380,140110358263,140110387720,140110357449,140110348263,140110380857,140110357022,140110334193,140110390695,140110348564,140110364396,140110362060,140110278902,140110360364,140110263037,140110366547,140110320108,140110372638,140110387248,140110367036,140110311884,140110405234,140110387712,140110400646,140110378178,140110393130,140110389009,140110348935,140110409990,140110413893,140110392454,140110253282,140110406587,140110367992,140110370968,140110367770,140110308838,140110387501,140110402408,140110361497,140110366632,140110365928,140110352238,140110406996,140110401030,140110382733,140110361514,140110363598,140110382800,140110387432,140110367208,140110391181,140110374800,140110370938,140110399914,140110253288,140110355287,140110405166,140110301171,140110358373,140110286761,140110364341,140110399265,140110352528,140110358931,140110358946,140110362374,140110362380,140110366428,140110369259,140110369263,140110369271,140110369300,140110378184,140110378198,140110378199,140110378209,140110382307,140110382320,140110382353,140110399571,140110399585,140110399595,140110402205,140110410470,140110413890,140110413896,140110413899,140110361487,140110361821,140110361829,140110361833,140110361839,140110363852,140110363880,140110363562,140110363564,140110363568,140110363569,140110363577,140110366995,140110367005,140110367011,140110367024,140110367026,140110367027,140110367028,140110370953,140110370955,140110368536,140110368595,140110368596,140110368622,140110378228,140110378246,140110385961,140110385967,140110385978,140110385981,140110385982,140110385983,140110386327,140110386333,140110386335,140110386339,140110386341,140110386346,140110386512,140110386518,140110386522,140110386535,140110388078,140110388069,140110388213,140110388226,140110388232,140110391105,140110390744,140110390745,140110390761,140110390762,140110390763,140110390765,140110390774,140110392504,140110392535,140110392544,140110392549,140110395496,140110399232,140110399233,140110399234,140110399240,140110399241,140110399242,140110399244,140110399247,140110399248,140110399249,140110399253,140110399254,140110399275,140110399611,140110399617,140110399620,140110399635,140110401637,140110401642,140110401649,140110401654,140110401660,140110401661,140110401666,140110401670,140110401671,140110407014,140110407015,140110407021,140110407022,140110407023,140110407026,140110407028,140110407030,140110407034,140110407039,140110407040,140110410275,140110410287,140110410288,140110410292,140110410298,140110410299,140110410304,140110410346,140110410349,140110409492,140110409652,140110412200,140110366621,140110353688,140110325996,140110364414,140110408994,140110372839,140110309210,140110409188,140110382424,140110359342,140110249011,140110278924,140110373685,140110378472,140110378484,140110387365,140110387375,140110388725,140110388194,140110388200,140110393569,140110399693,140110407106,140110407131,140110404870,140110383628,140110383643,140110383652,140110384609,140110384994,140110377424,140110383564,140110386447,140110386449,140110386458,140110386460,140110388084,140110357261,140110377102,140110377105,140110378298,140110378306,140110378310,140110403136,140110393722,140110303498,140110394367,140110396890,140110361572,140110361577,140110361580,140110361590,140110361606,140110362073,140110362140,140110362151,140110362152,140110362158,140110375027,140110375031,140110375044,140110395570,140110395576,140110395604,140110371426,140110377082,140110377092,140110377101,140110377114,140110377115,140110378297,140110378315,140110378325,140110378328,140110378331,140110360462,140110364754,140110378126,140110378538,140110378549,140110378574,140110393522,140110393557,140110401693,140110405131,140110405323,140110409007,140110409015,140110410111,140110410127,140110366971,140110370939,140110383478,140110386313,140110387306,140110267760,140110390089,140110262914,140110366988,140110386837,140110386839,140110324449,140110357161,140110357186,140110363732,140110369252,140110383578,140110383589,140110383603,140110383678,140110384539,140110372977,140110358492,140110364329,140110360418,140110360440,140110361019,140110353342,140110367248,140110379607,140110386020,140110385362,140110385838,140110385828,140110386176,140110386188,140110386508,140110386690,140110388203,140110392160,140110389468,140110399813,140110400708,140110400561,140110400572,140110400578,140110400579,140110402289,140110402796,140110405427,140110405438,140110405439,140110405441,140110405455,140110396039,140110366562,140110393302,140110409285,140110409319,140110409679,140110409752,140110369289,140110373302,140110385737,140110387841,140110387859,140110387867,140110368017,140110387543,140110393709,140110393993,140110382324,140110399774,140110401682,140110359416,140110360973,140110367172,140110383686,140110392109,140110392468,1401103… (truncated, 343702 characters total — see the official FDA record for the full value)
Recalling firm:
Acorn Stairlifts, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 2, 2016

2nd EXPANSION 5/31/2016 Roasted No Salt Ranch Sunflower Kernel, 45 lb. box. Product of USA, Manufactured by SunOpta, Crookston, MN

SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016

ARCACOCTFLGAIAILINKSKYLAMAMDMIMNMTNCNDNHNJNYOHOKORPASDTXVAWAWI
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-2266-2016
Lot/product code:
2nd EXPANSION 5/31/2016 PLot#: 8H5M25
Recalling firm:
SunOpta Food and Grain, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 2, 2016

2nd EXPANSION 5/31/2016 Blazin Hot sunflower kernel 1.2 oz. plastic bag. Product of USA, Manufactured by SunOpta, Crookston, MN

SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016

ARCACOCTFLGAIAILINKSKYLAMAMDMIMNMTNCNDNHNJNYOHOKORPASDTXVAWAWI
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-2262-2016
Lot/product code:
2nd EXPANSION 5/31/2016 PLot#: 34215159, 34215160, 34215161, 34215170, 34215173, 34215174, 34215175, 34215176, 34215177, 34215180, 34215181.
Recalling firm:
SunOpta Food and Grain, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 2, 2016

2nd EXPANSION 5/31/2016 Product shipped OUS only. Spitz Dill Pickle Sunflower Kernel, 100g plastic bag, UPC 69579-21001. Product of USA,

SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016

ARCACOCTFLGAIAILINKSKYLAMAMDMIMNMTNCNDNHNJNYOHOKORPASDTXVAWAWI
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-2268-2016
Lot/product code:
2nd EXPANSION 5/31/2016 PLot#: 07-09-16C2, 09-10-16B, 09-11-16A, 11-10-16B, 11-10-16C, 01-07-17A.
Recalling firm:
SunOpta Food and Grain, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 2, 2016

EXPANDED 5/18/2016 DAKOTA STYLE Salted Caramel sunflower kernel 2000 lbs. Poly Lined - Poly Woven Tote, Product of USA, Manufactured by SunOpta, Crookston, MN

SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016

ARCACOCTFLGAIAILINKSKYLAMAMDMIMNMTNCNDNHNJNYOHOKORPASDTXVAWAWI
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-2261-2016
Lot/product code:
EXPANDED 5/18/2016 PLot# / Child Lot# / Expiration 8C6M31 / 37260915128 / 6/29/16 2nd EXPANSION 5/31/2016 PLot#: 8F5M03, 8H5M12.
Recalling firm:
SunOpta Food and Grain, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 2, 2016

1. Roasted Not Salted Sunflower Kernel, 5 lbs (2.25 kgs) box, Manufactured by SunOpta, Crookston, MN; 2. Roasted Not Salted Sunflower Kernels, 25 lbs (11.34 kgs) poly lined paper bag, Manufactured by SunOpta, Crookston, MN; 3. Roasted Not Salted SL-80 Sunflower Kernels, 45 lbs vacuum packed bag in box, Manufactured by SunOpta, Crookston, MN; 4. Roasted Not Salted Sunflower Kernel, 50 lbs. bag, Product of USA, Manufactured by SunOpta, Crookston, MN; EXPANDED 5/18/2016 Roasted Not Salted Sunflower Kernel, 2000 lbs. Poly Lined - Poly Woven Tote, Product of USA, Manufactured by SunOpta, Crookston, MN;

SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016.

ARCACOCTFLGAIAILINKSKYLAMAMDMIMNMTNCNDNHNJNYOHOKORPASDTXVAWAWI
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-2259-2016
Lot/product code:
5 lb PLot # / Child Lot # / Expiration: 8B6M02 / 37260335027 / 2/2/2017 25 lb PLot # / Child Lot # / Expiration: 8B6M02 / 37260335021 / 4/26/2016 45 lb PLot # / Child Lot # / Expiration: 8B6M02378737 / 37260325127 / 2/1/2017 8B6M02378737 / 37260325128 / 2/1/2017 8B6M02378737 / 37260325140 / 2/1/2017 8B6M02378737 / 37260325141 / 2/1/2017 8b6m01378108 / 37260325001 / 2/1/2017 8B6M01378108 / 37260325002 / 2/1/2017 8B6M01378108 / 37260325003 / 2/1/2017 8B6M03375785 / 37260345100 / 2/3/2017 8B6M03 / 37260325151 / 2/1/2017 8B6M02376004 / 37260325102 / 2/1/2017 8B6M02376004 / 37260325103 / 2/1/2017 8B6M02376004 / 37260325122 / 2/1/2017 8B6M02376004 / 37260325123 / 2/1/2017 8B6M08376004 / 37260395012 / 2/8/2017 8B6M08376004 / 37260395013 / 2/8/2017 8B6M08376004 / 37260395013/ 2/8/2017 8B6M08376004 / 37260395014 / 2/8/2017 8B6M08376004 / 37260395015 / 2/8/2017 8B6M02377709 / 37260325004 / 2/1/2017 8B6M02377709 / 37260325005 / 2/1/2017 8B6M02377709 / 37260325007 / 2/1/2017 8B6M02377709 / 37260325008 / 2/1/2017 8B6M02377709 / 37260325009 / 2/1/2017 8B6M02377709 / 37260325013 / 2/1/2017 8B6M02377709 / 37260325014 / 2/1/2017 8B6M02377709 / 37260325022 / 2/1/2017 8B6M02377709 / 37260325026 / 2/1/2017 8B6M02377709 / 37260325043 / 2/1/2017 8B6M02377709 / 37260325044 / 2/1/2017 8B6M02377709 / 37260325045 / 2/1/2017 8B6M02377709 / 37260325061 / 2/1/2017 8B6M02377709 / 37260325062 / 2/1/2017 8B6M02377709 / 37260325076 / 2/1/2017 8B6M02377709 / 37260325081 / 2/1/2017 8B6M02377709 / 37260325086 / 2/1/2017 8B6M02377709 / 37260465026 / 2/15/2017 50 lb PLot # / Child Lot # / Expiration: 8b6m02 / 37260335023 / 4/26/2016 8B6M02 / 37260335024 / 4/26/2016 8B6M02 / 37260335034 / 4/26/2016 8B6M02 / 37260335035 / 4/26/2016 8B6M02 / 37260335036 / 4/26/2016 8B6M02 / 37260335037 / 4/26/2016 8B6M08 / 37260395018 / 5/2/2016 8B6M08 / 37260395019 / 5/2/2016 8B6M08 / 37260395020 / 5/2/2016 8B6M08379415 / 37260395008 / 5/2/2016 8B6M08379415 / 37260395009 / 5/2/2016 8B6M08379415 / 37260395010 / 5/2/2016 8B6M08379415 / 37260395011 / 5/2/2016 EXPANDED 5/18/2016 5 LB Bag in a Box PLot# / Child Lot# / Expiration 8B6M23 / 37260545310 / 5/23/16 8C6M07 / 37260675075 / 6/5/16 8C6M21 / 37260815182 / 6/19/16 25 LB Poly Lined Paper Bag PLot# / Child Lot# / Expiration 8B6M24 / 37260555107 / 5/24/16 8B6M24 / 37260555108 / 5/24/16 8B6M24 / 37260555109 / 5/24/16 8C6M01 / 37260615030 / 5/30/16 8C6M01 / 37260615031 / 5/30/16 8C6M01 / 37260615032 / 5/30/16 8C6M01 / 37260615033 / 5/30/16 8C6M01 / 37260615034 / 5/30/16 8C6M09 / 37260685319 / 6/6/16 8C6M09 / 37260685327 / 6/6/16 8C6M09 / 37260685332 / 6/6/16 8C6M21 / 37260815004 / 6/19/16 8C6M21 / 37260815005 / 6/19/16 8C6M21 / 37260815006 / 6/19/16 8C6M21 / 37260815007 / 6/19/16 8C6M30 /37260905093 / 6/28/16 8C6M30 / 37260905094 / 6/28/16 8C6M30 / 37260905110 / 6/28/16 8C6M30 / 37260905111 / 6/28/16 8C6M30 / 37260905112 / 6/28/16 8C6M30 / 37260905118 / 6/28/16 8C6M30 / 37260905136 / 6/28/16 8C6M30 / 37260905137 / 6/28/16 8C6M30 / 37260905138 / 6/28/16 8D6M20 / 37261115200 / 7/19/16 8D6M20 / 37261115201 / 7/19/16 45 LB Vac Pac Bag in Box PLot# / Child Lot# / Expiration 4B6M22 / 37260535043 / 2/21/17 4B6M22 / 37260535056 / 2/21/17 4B6M22 / 37260535057 / 2/21/17 8B6M17 / 37260485054 / 2/16/17 8B6M22337497 / 37260535004 / 2/21/17 8B6M22337497 / 37260535008 / 2/21/17 8B6M22337497 / 37260535010 / 2/21/17 8B6M22377497 / 37260535001 / 2/21/17 8B6M22377497 / 37260535002 / 2/21/17 8B6M22377497 / 37260535003 / 2/21/17 8B6M22380161 / 37260535012 / 2/21/17 8B6M22380161 / 37260535013 / 2/21/17 8B6M22380161 / 37260535019 / 2/21/17 8C6M14381336 / 37260745000 / 3/14/17 8C6M14381336 / 37260745001 / 3/14/17 8C6M14381336 / 37260745002 / 3/14/17 8C6M14381336 / 37260745003 / 3/14/17 8C6M14381336 / 37260745004 / 3/14/17 8C6M14381336 / 37260745005 / 3/14/17 8C6M15 / 37260745012 / 3/14/17 8C6M21 / 37260815000 / 3/21/17 8C6M21 / 37260815001 / 3/21/17 8C6M21 / 37260815002 / 3/21/17 8C6M21 / 37260815003 / 3/21/17 8C6M28382554 / 37260885003 / 3/28/17 8C6M28382554 / 37260885004 / 3/28/17 8C6M28382554 / 37260885005 / 3/28/17 8C6M28382554 / 37260885006 / 3/28/17 8C6M28384103 / 37260885007 / 3/28/17 8C6M30383782 / 37260905042 / 3/30/17 8C6M30383782 / 37260905060 / 3/30/17 8C6M30383782 / 37260905061 / 3/30/17 8C6M30384660 / 37260905063 / 3/30/17 8C6M30384660 / 37260905073 / 3/30/17 8C6M30384660 / 37260905074 / 3/30/17 8C6M30384660 / 37260905075 / 3/30/17 8D6M04385334 / 37260955001 / 4/4/17 8D6M04385334 / 37260955002 / 4/4/17 8D6M04385334 / 37260955004 / 4/4/17 8D6M04385334 / 37260955005 / 4/4/17 8D6M04385334 / 37260955009 / 4/4/17 8D6M04385334 / 37260955010 / 4/4/17 8D6M04385334 / 37260955012 / 4/4/17 8D6M04385334 / 37260955019 / 4/4/17 8D6M04385334 / 37260955020 / 4/4/17 8D6M04385334 / 37260955024 / 4/4/17 8D6M04385334 / 37260955025 / 4/4/17 8D6M04385334 / 37260955042 / 4/… (truncated, 24935 characters total — see the official FDA record for the full value)
Recalling firm:
SunOpta Food and Grain, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 2, 2016

2nd EXPANSION 5/31/2016 DAKOTA STYLE Ranch sunflower kernel 50 lb. plain bag. Product of USA, Manufactured by SunOpta, Crookston, MN

SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016

ARCACOCTFLGAIAILINKSKYLAMAMDMIMNMTNCNDNHNJNYOHOKORPASDTXVAWAWI
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-2263-2016
Lot/product code:
2nd EXPANSION 5/31/2016 PLot#: 8K5M18.
Recalling firm:
SunOpta Food and Grain, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 2, 2016

2nd EXPANSION 5/31/2016 Sunrich Naturals Chili Lime flavored Sunflower Kernels, packaged under the following sizes: 1. Net Wt. 1 oz. plastic bag, UPC 10304-01214; 2. Net Wt. 1.2 oz. (34g), UPC 10304-03214 . Product of USA. Distributed by Sunrich Consumer Brands, Hope, MN 56046

SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016

ARCACOCTFLGAIAILINKSKYLAMAMDMIMNMTNCNDNHNJNYOHOKORPASDTXVAWAWI
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-2269-2016
Lot/product code:
2nd EXPANSION 5/31/2016 1 oz. package PLot#: 34215155, 34215156, 34215159, 34215160, 34215166, 34215167. 1.2 oz. package PLot#: 34215168.
Recalling firm:
SunOpta Food and Grain, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 2, 2016

2nd EXPANSION 5/31/2016 Navitas Naturals, Superfood GOJI, Tangy berry, acai Nut Bar, 1.4 oz., UPC 11961-02028 Distributed by Navitas Naturals, Novato, CA 94948.

SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016

ARCACOCTFLGAIAILINKSKYLAMAMDMIMNMTNCNDNHNJNYOHOKORPASDTXVAWAWI
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-2271-2016
Lot/product code:
2nd EXPANSION 5/31/2016 PLot# 80316055
Recalling firm:
SunOpta Food and Grain, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 2, 2016

2nd EXPANSION 5/31/2016 Product shipped OUS only. Light Salt Sunflower Kernel, 5 kg / 11 lb. box. Product of USA, Manufactured by SunOpta, Crookston, MN

SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016

ARCACOCTFLGAIAILINKSKYLAMAMDMIMNMTNCNDNHNJNYOHOKORPASDTXVAWAWI
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-2265-2016
Lot/product code:
2nd EXPANSION 5/31/2016 PLot#: 8L5M10
Recalling firm:
SunOpta Food and Grain, Inc.
View official FDA record (opens in a new tab)