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Recalls affecting Georgia

Data last updated: September 7, 2026 at 12:15 AM UTC

17,234 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 Mendietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

Full report
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 AliveMoringa Leaf Powder

Potential to be contaminated with Salmonella

Full report
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. Braun0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

Full report
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 ValueOrganic Triple Berry Blend

Possible E. Coli Contamination

Full report
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

Full report
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

LipofitLipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Full report
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

KofinasGarlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

Full report
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 TemptationsChocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

Full report
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 SproutsRobust Radish Mix, 5oz Cups

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

Full report
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

MartinaMangoes

Potential contamination with Salmonella

Full report
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)
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
Full report

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 Premium Teriyaki Marinade, 1 oz (28 g), polypropylene and clamshell style card, 12 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-2079-2016
Lot/product code:
Cases coded 2014-2015, if not visible all lots; UPC: 0-34795-00036-5.
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
Full report

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 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
Full report

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
Full report

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
Full report

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.

ALL 50 STATES
Full report

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

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 #:
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.

ALL 50 STATES
Full report

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 IIModerate risk
FoodAllergenUndeclaredRecalled April 26, 2016

White Cupcakes with Blue Icing, UPC #10074865110164

Not listed on the label allergen; Peanut Protein

Full report

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

Recall #:
F-1516-2016
Lot/product code:
Blue Icing - Code D16-097
Recalling firm:
Dessert Innovations II Candy Divison
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenUndeclaredRecalled April 26, 2016

White Cupcakes with Yellow Icing, UPC #10074865110157

Not listed on the label allergen; Peanut Protein

Full report

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

Recall #:
F-1517-2016
Lot/product code:
Yellow Icing - Code D16-095 & D-16-096
Recalling firm:
Dessert Innovations II Candy Divison
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenUndeclaredRecalled April 26, 2016

White Cupcakes with White Icing, UPC #10074865110102

Not listed on the label allergen; Peanut Protein

Full report

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

Recall #:
F-1515-2016
Lot/product code:
White Icing - Code D16-095
Recalling firm:
Dessert Innovations II Candy Divison
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenUndeclaredRecalled April 26, 2016

White Cupcakes with Pink Icing, UPC #10074865110140

Not listed on the label allergen; Peanut Protein

Full report

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

Recall #:
F-1514-2016
Lot/product code:
Pink Icing - Code D16-097 & D16-102
Recalling firm:
Dessert Innovations II Candy Divison
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

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

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

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 Roasted No Salt Sweet Onion & White Cheddar 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

Full report

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

Recall #:
F-2267-2016
Lot/product code:
2nd EXPANSION 5/31/2016 PLot#: 8H5M26
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 HEMP, Creamy Peanut, hemp Nut Bar, 1.4 oz., UPC 11961-02030 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

Full report

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

Recall #:
F-2272-2016
Lot/product code:
2nd EXPANSION 5/31/2016 PLot# 80316054
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

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. Chili Limon 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

Full report

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

Recall #:
F-2264-2016
Lot/product code:
2nd EXPANSION 5/31/2016 PLot#: 8L5M16
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 MACA, Sweet Maple maca Nut Bar, 1.4 oz., UPC 11961-02024 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

Full report

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

Recall #:
F-2273-2016
Lot/product code:
2nd EXPANSION 5/31/2016 PLot# 80316053
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

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

DAKOTA STYLE SAVORY BACON 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

Full report

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

Recall #:
F-2260-2016
Lot/product code:
PLot# / Child Lot# / Expiration 8B6M09 / 37260405180 / 5/3/2016 8B6M09 / 37260405181 / 5/3/2016 EXPANDED 5/18/2016 PLot# / Child Lot# / Expiration: 8D6M01 / 37260925033 / 6/30/16 2nd EXPANSION 5/31/2016 PLot#: 8F5M09, 8H5M12, 8I5M21, 8J5M27, 8A6M13.
Recalling firm:
SunOpta Food and Grain, Inc.
View official FDA record (opens in a new tab)