BIGNOPE
Ko-fi

Recalls affecting Massachusetts

Data last updated: September 8, 2026 at 1:13 PM UTC

17,003 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

▸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 Alive — Moringa 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. Braun — 0.9% 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 Value — Organic 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

Lipofit — Lipofit 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

Kofinas — Garlic 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 Temptations — Chocolatey 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 Sprouts — Robust 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

Martina — Mangoes

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)
NewestOldest
High riskLow riskAll
Wording
Class IIModerate risk
DrugRecalled November 17, 2016

Testosterone Cypionate/Propionate, 200 mg/50 mg/mL, (5 ML). Compounded by Tri-Coast Pharmacy

Not guaranteed to be germ-free

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-0303-2017
Lot/product code:
Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 07132016D (01/09/2017), 11072016B (05/06/2017).
Recalling firm:
Tri-Coast Pharmacy
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 17, 2016

Calcium Gluconate 10% Injection (30 ML). Compounded by Tri-Coast Pharmacy

Not guaranteed to be germ-free

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-0254-2017
Lot/product code:
Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 08172016A (02/13/2017).
Recalling firm:
Tri-Coast Pharmacy
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 17, 2016

HCG 5,000 IU Vial. Compounded by Tri-Coast Pharmacy.

Not guaranteed to be germ-free

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-0261-2017
Lot/product code:
Lot codes: 06222016D, 06062016C, 07192016C07062016A, 08182016B, 08112016A, 08012016A, 09282016A, 09122016D, 10182016C, 11042016B, 11012016F; Exp. 11/16
Recalling firm:
Tri-Coast Pharmacy
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 17, 2016

Quad Mix, Alprostadil/Phentolamine/Papaverine/Atropine 18mcg/1mg/1.8mg/0.02mg/ml, (1 ML). Compounded by Tri-Coast Pharmacy

Not guaranteed to be germ-free

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-0286-2017
Lot/product code:
Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 07252016E (09/04/2016), 09142016A (09/29/2016), 07192016E (09/01/2016), 07052016B (08/04/2016).
Recalling firm:
Tri-Coast Pharmacy
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 17, 2016

TriMix, Alprostadil/Phentolamine/Papaverine 10mcg/0.5mg/30mg/mL, (1 ML). Compounded by Tri-Coast Pharmacy

Not guaranteed to be germ-free

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-0310-2017
Lot/product code:
Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 07152016C (08/22/2016), 09292016A (11/06/2016).
Recalling firm:
Tri-Coast Pharmacy
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 17, 2016

TriMix, Alprostadil/Phentolamine/Papaverine 20mcg/1mg/30mg/mL, (1 ML). Compounded by Tri-Coast Pharmacy

Not guaranteed to be germ-free

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-0312-2017
Lot/product code:
Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 06152016D (07/17/2016), 07272016D (09/08/2016), 10252016I (12/09/2016), 10172016A (11/24/2016), 10202016A (11/24/2016).
Recalling firm:
Tri-Coast Pharmacy
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 17, 2016

Quad Mix, Alprostadil/Phentolamine/Papaverine/Atropine 10mcg/1mg/9mg/0.1mg/ml, (1 ML). Compounded by Tri-Coast Pharmacy

Not guaranteed to be germ-free

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-0281-2017
Lot/product code:
Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 06162016B (07/17/2016).
Recalling firm:
Tri-Coast Pharmacy
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 18, 2016

ddR Formula B X-ray System, Model ddR Formula B X-ray system used for imaging

Potential for bucky (the part that holds the grid and is moveable to position the patient) moving unexpectedly.

ALL 50 STATES
▸Full report

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

Recall #:
80981
Lot/product code:
Serial Numbers within U.S.A commerce - 1302002, 1302003, 1302005, 1302009, 1302011, 1402001, 1402002, 1402006, 1402007, 1402008, 1402009, 1402011, 1402012, 1402015, 1502001, 1502002, 1502004, 1502005, 1502006, 1502007, 1602001, 1602002, 1602003, 1602005, 1602006, 1602007 & 1602008   Serial Numbers Outside of U.S.A commerce - 1402005, 1402017, 1502009, 1502010, 1502011, 1302004, 1302006, 1302007, 1302008, 1302010, 1402003, 1402004, 1402010, 1402013, 1402014, 1402016, 1502008 & 1602004
Recalling firm:
Swissray Medical
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 1, 2017

Alpha Air 6 ENT Microscope Microscope examination of the human ear, nose, and throat.

The microscope may tip over if attachments are fully extended in one line and there is an attempt to move the device not by the handles mounted on the post.

ALL 50 STATES
▸Full report

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

Recall #:
79362
Lot/product code:
Model Number 6 ENT
Recalling firm:
Seiler Instr. & Mfg. Co. Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 6, 2017

Color contact lenses labeled under the following brands: Diamond, Fierce, Ambition, Circle Collection, Lunatic, Fright, Desire and See Clear.

Sterility and Misbranding: Lenses may not be sterile and may be labeled with erroneous lot numbers and expiry dates.

ALL 50 STATES
▸Full report

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

Recall #:
76279
Lot/product code:
All lots of lenses sold between 10/31/2013 to 10/31/2016
Recalling firm:
The See Clear Company
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 11, 2017

L-Varlock Cage/Trial Implant Holder, Reference HD0060, Kisco International, France. Product Usage: The L-Varlock Lumbar Cage is indicated for intervertebral body fusion procedures in skeletally mature patients with degenerative disc disease (DDD) of the lumbar spine at one or two contiguous levels from L2-S1. DDD is defined as discogenic pain with degeneration of the disc confirmed by history and radiographic studies. These DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). L-Varlock Lumbar implants are to be used with autogenous bone graft and implanted via an open posterior approach. L-Varlock Lumbar implant is to be used with supplemental fixation. Patients should have at least six (6) months of non-operative treatment prior to treatment with an intervertebral cage.

Firm received a complaint of the tip holder breaking during use.

ALL 50 STATES
▸Full report

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

Recall #:
76494
Lot/product code:
Batch number: 15486
Recalling firm:
Kiscomedica S.A.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 11, 2017

Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a quantitative imaging software application intended to be used to process digital image files.

Ortho Kinematics Inc. sent a Notice of Correction to Released Testing Results, Radiological Read Report for the Vertebral Motion Analyzer (VMA) test because it contained an error. The error occurred due to a software bug that has been corrected.

ALL 50 STATES
▸Full report

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

Recall #:
80680
Lot/product code:
UDI: 00868579000209
Recalling firm:
Ortho Kinematics, Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled January 18, 2017

Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50 unit dose cups per case (NDC 66689-047-50), Rx only, Xact Dose, Manufactured by VistaPharm, Largo, FL 33771.

Defective Container: Leakage of unit dose cups that may occur at the seal.

ALAZCACOCTFLGAHIIAILINKSKYLAMAMIMNMOMSNCNENHNJNMNYOHOKORPATNTXUTVAWAWIWV
▸Full report

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

Recall #:
D-0469-2017
Lot/product code:
Lot #'s: 437600, Exp 07/17; 447100, Exp 10/17
Recalling firm:
VistaPharm, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 3, 2017

HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The HeartWare Ventricular Assist System (VAS) is designed for in-hospital and out-of-hospital settings, including transportation via fix-wing aircraft or helicopter

Product recall of all HVAD Controllers currently on the market and to exchange them for the next generation HVAD Controller (Controller2.0)

ALL 50 STATES
▸Full report

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

Recall #:
76600
Lot/product code:
HeartWare HVAD System Controller Product numbers: 1401US, 1401XX, 1403US, 1407XX, and 1400 with the serial Number(s) lower than CON300000 HeartWare HVAD DC Adapter Product number: 1435  .
Recalling firm:
Heartware
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Pepper Jack Cheese packaged as: (a) Troyer Pepper Jack EW Halfmoon, Item 10840, 8 oz, UPC 49646936106 (b) Troyer Pepper Jack EW Full Moon, Item 10841, 8 oz, UPC 49646936069

Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1710-2017
Lot/product code:
Lot Numbers: (a) Best if used by: 02/28/2017 through 08/14/2017 (b) Best if used by: 02/28/2017 through 08/14/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Grand Butterkase Cheese packaged as: (a) AMISH CLASSICS Grand Butterkase, Item 65209, 6 lbs, UPC 828654652090 (b) AMISH CLASSICS Grand Butterkase RW Fullmoon, Item 65241, 12 lbs, no UPC (c) AMISH CLASSICS Grand Butterkase EW Fullmoon, Item 65245, 8 oz, UPC 828653652458

Sample of product collected by the State Department of Agriculture tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1699-2017
Lot/product code:
Lot Numbers: (a) Best if used by: 02/28/2017 through 08/14/2017 (b) Best if used by: 02/28/2017 through 08/14/2017 (c) Best if used by: 02/28/2017 through 08/14/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Havarti Cheese Packaged as: (a) AMISH CLASSICS Deli Made EZ Havarti .75oz St Pk Slice, Item 71554, 1.5 lbs, UPC 82853715542

Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1708-2017
Lot/product code:
Lot Numbers: (a) Best if Used by: 5/3/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Provolone Cheese packaged as: (a) Santino Deli Made EZ Provolone St Pck .75oz Slice, Item 58554, 1.5 lbs, UPC 828828653585541 (b) Deli Made EZ Provolone St Pck .5oz Slice, Item 58555, 1.5 lbs, UPC 828653585558 (c) Duck Deli Provolone Stk Pck .75oz Slice, Item 58747, 1.5 lbs, UPC 828653587476 (d) La Rosa's Pizzaria Provolone St Pk .667oz, Item 58774, 2.25 lbs, UPC 828653587743

Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1706-2017
Lot/product code:
Lot Numbers: (a) Best if Used by: 3/28/2017 (b) Best if Used by: 3/28/2017 (c) Best if Used by: 004-17 (d) Best if Used by: 004-17
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Monterey Jack Cheese packaged as: (a) AMISH CLASSICS Deli Made EZ Monterey Jack St Pk .75 oz Slice, Item 03554, 1.5 lbs, UPC 828653035541

Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1704-2017
Lot/product code:
Lot Numbers: (a) Best if Used by: 3/28/2017, 5/3/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Colby Cheese packaged as follows: (a) AMISH CLASSICS, DELI HORN, Item 55209, NET WT 6 LBS, UPC 0 08 28653 55209 3 (b) AMISH CLASSICS, FULLMOON(R), Item 55241, approximately 8 oz, UPC 828653552413 (c) AMISH CLASSICS EW FULL MOON, ITEM 55245, 8 oz, UPC 828653552451 (d) 8/2# RW Deli Readi Colby Mini Cheese Slices, ITEM 55831, 2 lbs., UPC 634660 628597 (e) Deli Made EZ(R) Slices, NET WT1.5 LB (681g), Item 55553, UPC 8 28653 55554 4 (f) Meijer Colby Cheese DELI HORN, Item 55755, 6 lbs., no UPC (g) Amish Classics Colby RW Halfmoon, Item 55244, 8 oz, no UPC (h) Meijer Colby EW Halfmoon, Item 55758, 8 oz, UPC 7 13733 34047 2 (i) RW Deli Readi Colby 1/2 Moon Slices, Item 55830, 1 lb, UPC 6 34660 62872 6 (j) Old Tyme Colby EW Halfmoon, Item 55703, 8 oz, UPC 8 28653 10555 8 (k) AMISH CLASSICS Colby Longhorn, Item 55523, 15 lbs, no UPC (l) Dietz & Watson Colby Mini Horn, Item 55740, 6 lbs, no UPC (m) Troyer Colby EW Halfmoon, Item 55840, 8 oz, UPC 04964693609 (n) Troyer Colby EW Full Moon, Item 55841, 8 oz, UPC 049646936045 (o) Troyer Colby RW Halfmoon, Item 55842, 8 oz, no UPC

Sample of product collected by the State Department of Agriculture tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1694-2017
Lot/product code:
(a) Lot Numbers: Sell By: 02/28/2017 through 08/14/2017 (b) Lot Numbers: Best if Used By: 02/28/2017 through 08/14/2017 (c) Lot Numbers: Best if Used By: 02/28/2017 through 08/14/2017 (d) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (e) Lot number 335-16, Best if used by: 02/28/2017 through 08/14/2017 (f) Lot Numbers: Sell by Date: 05/02/2017, 02/28/2017 through 08/14/2017 (g) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (h) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (i) Lot Numbers: USE BY: 02/28/2017 through 08/14/2017 (j) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (k) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (l) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (m) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (n) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017 (o) Lot Numbers: Best if used by: 02/28/2017 through 08/14/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Colby Jack Cheese packaged as follows: (a) m markets of Meijer(R), NET WT 6 LBS (2.72 kg), Item 18755, UPC 71091718755 (b) Amish classics Colby Jack RW Halfmoon, Item 18244, 8 oz, no UPC (c) Meijer Colby Jack EW Halfmoon Chunk, Item 18758, 8 oz, UPC 713733340588 (d) Amish Classics Colby Jack RW Fullmoon, Item 18241, 8 oz, no UPC (e) Amish Classics Colby Jack EW Fullmoon, Item 18245, 8 oz, 828653182450 (f) Deli Readi Colby Jack 1/2 Moon Slices, Item 18830, 1 lb, UPC 6 34660 62875 7 (g) Amish Classics Colby Jack Mini Horn, Item 18209, 6 lbs, no UPC (h) LIPARI OLD TYME Colby Jack EW Halfmoon, Item 18703, 8 oz, UPC 094776102211 (I) Deli Readi Colby Jack St Pk 1oz Mn Hrn Slice, Item 18831, 2 lbs, UPC 634660628603 (j) Dietz & Watson Colby Jack Mini Horn, Item 18740, 6 lbs, no UPC (k) Winder Farms Colby Jack St Pk .75oz Slice, Item 18790, 1 lb, UPC 828653187905

Sample of product collected by the State Department of Agriculture tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1695-2017
Lot/product code:
Lot Numbers: (a) Sell by Date: 02/28/2017 through 08/14/2017 (b) Best if used by: 02/28/2017 through 08/14/2017 (c) Best if used by: 02/28/2017 through 08/14/2017 (d) Best if used by: 02/28/2017 through 08/14/2017 (e) Best if used by: 02/28/2017 through 08/14/2017 (f) USE BY: 02/28/2017 through 08/14/2017 (g) Best if used by: 02/28/2017 through 08/14/2017 (h) Best if used by: 02/28/2017 through 08/14/2017 (i) Best if used by: 02/28/2017 through 08/14/2017 (j) Best if used by: 02/28/2017 through 08/14/2017 (k) Best if used by: 02/28/2017 through 08/14/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Marble Cheese packaged as: (a) Troyer Marble EW Halfmoon, Item 18840, 8 oz, UPC 49646936113 (b) Troyer Marble EW Full Moon, Item 18841, 8 oz, UPC 49646936052 (c) Troyer Marble RW Halfmoon, Item 18842, 8 oz, no UPC

Sample of product collected by the State Department of Agriculture tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1701-2017
Lot/product code:
Lot Numbers: (a) Best if used by: 02/28/2017 through 08/14/2017 (b) Best if used by: 02/28/2017 through 08/14/2017 (c) Best if used by: 02/28/2017 through 08/14/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Mozzarella Cheese packaged as: (a) Deli Made EZ Mozzarella St Pk .75oz Slice, Item 11553, 1.5 lbs, UPC 828653105558

Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1705-2017
Lot/product code:
Lot Numbers: (a) Best if Used by: 322-16, 333-16
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Jalapeno Jack cheese packaged as follows: (a) AMISH CLASSICS Jalapeno Jack Mini Horn, Item 10209, 6 lbs, No UPC (b) AMISH CLASSICS Jalapeno Jack RW Fullmoon, Item 10241, 12 lbs, no UPC (c) AMISH CLASSICS Jalapeno Jack RW Halfmoon, Item 10244, 12 lbs, no UPC (d) AMISH CLASSICS Jalapeno Jack EW Fullmoon, Item 10245, 8 oz, UPC 828653102458 (e) AMISH CLASSICS Jalapeno Jack Cheese, Item 10311, 10 lbs, no UPC 10 lbs, no UPC (f) Deli Made EZ Jalapeno Jack St Pk .75 oz Slice, Item 10553, 1.5 lbs, no UPC (g) Deli Made EZ Jalapeno Jack St Pk .75 oz Slice, Item 10554, 1.5 lbs, UPC 828653105541 (h) Deli Made EZ Jalapeno Jack St Pk .5 oz Slice, Item 10555, 1.5 lbs, UPC 828653105558 (i) LIPARI Old Tyme Jalapeno Jack EW Halfmoon, Item 10703, 8 oz, UPC 94776102303 (k) Sutters Quality Foods Jalapeno Jack St Pk .75oz Slice, Item 10812, 1.5 lbs, UPC 828653108122 (l) Sutters Quality Foods Jalapeno Jack Loaf, Item 10815, 5 lbs, no UPC (n) Winder Farms Jalapeno Jack St Pk .75oz Slice, Item 10790, 1 lb, UPC 828653107903

Sample of product collected by the State Department of Agriculture tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1696-2017
Lot/product code:
Lot Numbers: (a) Best if used by: 02/28/2017 through 08/14/2017 (b) Best if used by: 02/28/2017 through 08/14/2017 (c) Best if used by: 02/28/2017 through 08/14/2017 (d) Best if used by: 02/28/2017 through 08/14/2017 (e) Best if Used by: 4/18/2017 (f) Best if Used by: 003-17 (g) Best if Used by: 3/17/2017, 5/3/2017 (h) Best if Used by: 3/28/2017, 3/30/2017, 5/18/2017 (i) Best if Used by: 5/29/2017 (j) Best if Used by: 2/28/2017, 5/16/2017 (k) Best if Used by: 5/9/2017 (l) Best if Used by: 5/3/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 4, 2017

Jalapeno Colby Jack Cheese packaged as: (a) AMISH CLASSICS Jalapeno Colby Jack EW Fullmoon, Item 17245, 8 oz., UPC 828653102458(b) AMISH CLASSICS Jalapeno Colby Jack Mini Horn, Item 17209, 6 lbs., No UPC

Sample of product collected by the State Department of Agriculture tested positive for Listeria Monocytogenes

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸Full report

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

Recall #:
F-1698-2017
Lot/product code:
Lot Numbers: (a) Best if used by: 02/28/2017 through 08/14/2017 (b) Best if used by: 02/28/2017 through 08/14/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)