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Recalls affecting Tennessee

Data last updated: September 6, 2026 at 10:21 PM UTC

16,882 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
Wording
Class IHigh risk
DrugRecalled September 10, 2012

HYDROCODONE BITARTRATE and ACETAMINOPHEN TABLETS, USP, 10 mg/500 mg, 100-count bottle, Rx only, Mfg. for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-3888-21

Stronger than it should be (Multiple Ingredient) Drug: Confirmed customer complaints of oversized tablets resulting in stronger than it should be assays of both the hydrocodone and acetaminophen components.

ALL 50 STATES
Full report

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

Recall #:
D-057-2013
Lot/product code:
Lot number: C1440512A, Exp 12/13
Recalling firm:
Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 2, 2015

Zero Xtreme High Performance Fat Burner capsules, 30-count bottle, Distributed by Xtreme Z Distributors, Inc., Miami, FL 33180

Marketed Without an Approved NDA/ANDA: FDA sampling and analysis confirmed the presence of sibutramine and desmethylsibutramine.

ALL 50 STATES
Full report

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

Recall #:
D-1165-2016
Lot/product code:
Lot 1220062085, Exp. 09/16
Recalling firm:
XTREME Z DISTRIBUTORS INC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 13, 2015

Akttive High Performance Fat Burner Gold dietary supplement capsules, 30-count bottle, Distributed by Life and More, L.L.C., Doral, Florida

Marketed Without An Approved NDA/ANDA: Dietary supplements contains not listed on the label sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling.

ALL 50 STATES
Full report

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

Recall #:
D-0664-2016
Lot/product code:
Lot # 000815004400; Exp 12/17
Recalling firm:
Life and More LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 27, 2015

MIRACLE DIET 30 capsules, 30-count bottle, Manufactured Exclusively For: The One Minute Miracle Inc., UPC 7 538073516768.

Marketed Without An Approved NDA/ANDA: Miracle Diet 30 was found to contain not listed on the label phenolphthalein, a drug product once contained in over-the-counter laxatives but was taken off the U.S. market due to safety concerns, making this product an unapproved drug.

ALL 50 STATES
Full report

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

Recall #:
D-0230-2016
Lot/product code:
All lots through Expiration Date 04/15/2018
Recalling firm:
The One Minute Miracle Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 27, 2015

MIRACLE ROCK 48 capsules, packaged in 2 x 2-count blisters, 4-count capsules per carton, Manufactured Exclusively For: The One Minute Miracle Inc., UPC 0911312397354.

Marketed Without An Approved NDA/ANDA: Miracle Rock 48 was found to contain not listed on the label thiosildenafil, an analogue of an FDA approved drug for male erectile dysfunchtion making this product an unapproved drug.

ALL 50 STATES
Full report

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

Recall #:
D-0229-2016
Lot/product code:
All lots through Expiration Date 06/01/2018
Recalling firm:
The One Minute Miracle Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 23, 2015

APEXXX tablets, 300 mg, packaged in 1-count blister cards, Distributed Exclusively by: Nuway Distributors, LLC, Orlando, FL USA; UPC 7 05105 96361 7.

Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with sildenafil, an FDA approved drug for the treatment of male erectile dysfunction, making this an unapproved drug.

ALL 50 STATES
Full report

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

Recall #:
D-0667-2016
Lot/product code:
All lots
Recalling firm:
Nuway Distributors, LLC
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 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)
Class IHigh risk
DrugRecalled August 4, 2016

Bupivacaine Hydrochloride Inj., USP (2.5 mg/mL) 0.25%, packaged in 30 mL Single-dose Preservative-Free vials, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1159-02

Presence of particulate matter: Confirmed customer report for the presence of particulate matter within a single vial.

ALL 50 STATES
Full report

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

Recall #:
D-0218-2017
Lot/product code:
Lot # 59064DK, Exp. 11/17
Recalling firm:
Hospira Inc., A Pfizer Company
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled 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

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
FoodRecalled February 4, 2017

Provolone Cheese Salame packaged as: (a) Sutters Quality Foods Provolone Salame, Item 58814, 6 lbs, no UPC

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

Full report

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

Recall #:
F-1707-2017
Lot/product code:
Lot Numbers: (a) Best if Used by: 5/6/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 4, 2017

Muenster Cheese packaged as: (a) AMISH CLASSICS Muenster RW End Chunks, Item 61243, 12 lbs, no UPC (b) AMISH CLASSICS Muenster RW square, Item 61244, 8 oz, no UPC (c) Deli Made EZ Muenster St Pk .75 oz Slice, Item 61552, 1.5 lbs, UPC 828653615521 (d) Meijer Muenster EW Square, Item 61758, 8 oz, UPC 886926375735 (e) Old Tyme Muenster EW Square, Item 61703, 8 oz, UPC 94776102242

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

Full report

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

Recall #:
F-1703-2017
Lot/product code:
Lot Numbers: (a) Best if used by: 273-16, 319-16, 341-16 (b) Best if used by: 3/28/2017, 5/13/2017, 6/4/2017 (c) Best if used by: 328-16 (d) Best if used by: 3/28/2017, 5/13/2017, 6/10/2017 (e) Best if used by: 6/4/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 4, 2017

Farmers Cheese packaged as: (a) AMISH CLASSICS Farmers Cheese Mini Horn, Item 69209, 6 lbs, no UPC (b) Troyer Farmers EW Halfmoon, Item 69840, 8 oz, UPC 49646936137 (c) Troyer Farmers EW Full Moon, Item 69841, 8 oz, UPC 49646936083 (d) Troyer Farmers RW Halfmoon, Item 59842, 8 oz, no UPC

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

Full report

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

Recall #:
F-1700-2017
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 (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
FoodRecalled 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

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
FoodRecalled 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

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
FoodRecalled 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

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
FoodRecalled 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

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
FoodRecalled 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

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
FoodRecalled 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

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
FoodRecalled 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

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)
Class IHigh risk
FoodRecalled 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

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
FoodRecalled February 4, 2017

Cheddar Cheese packaged as: (a) AMISH CLASSICS Cheddar Mild Color, Item 28311, 10 lbs, No UPC (b) Deli Made EZ Cheddar Mild Stick, Item 28532, 4.5 lbs, no UPC (c) Deli Made EZ Cheddar Mild C St Pk .75oz Slice, Item 28545, 2 lbs, UPC 828653285458 (d) AMISH CLASSICS Deli Made EZ Cheddar St Pk .75oz Slice, Item 28553, 1.5 Lbs, no UPC (e) AMISH CLASSICS Deli Made EZ Cheddar Mild Stk Pk .5oz Slice, Item 28555, 1.54 lbs, UPC 828653285557 (f) Deli Readi Cheddar St Pk 1oz Slice, Item 28831, 2 lbs, UPC 634660628771 (g) Duck Deli Cheddar Mild Color Loaf, Item 28745, 5 lbs, no UPC (h) Duck Deli Cheddar st pk .75oz Slice, Item 28747, 1.5 lbs, UPC 828653287476 (i) Madison Valley Farms Cheddar St Pk .75oz Slice, Item 28769, 1.5 lbs, UPC 828653287698 (j) Sutters Quality Foods Cheddar St Pk .75oz Slice, Item 28812, 1.5 lbs, UPC 828653288126 (k) Sutters Quality Foods Cheddar Mild Color Loaf, Item 28815, 5 lbs, no UPC (l) Troyer Cheddar EW Full Moon, Item 28841, 8 oz, UPC 49646936076

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

Full report

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

Recall #:
F-1702-2017
Lot/product code:
Lot Numbers: (a) Best if Used by: 3/28/2017, 4/25/2017, 5/26/2017, 7/3/2017 (b) Best if Used by: 4/18/2017 (c) Best if Used by: 4/22/2017 (d) Best if Used by: 018-17 (e) Best if Used by: 3/10/2017, 4/22/2017 (f) Best if Used by: 2/28/2017, 5/4/2017 (g) Best if Used by: 273-16 (h) Best if Used by: 004-17, 358-16 (i) Best if Used by: 320-16 (j) Best if Used by: 5/18/2017 (k) Best if Used by: 4/18/2017 (l) 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
FoodRecalled 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

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
FoodRecalled 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

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)