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FDA food · drug · device recalls, merged

Before you eat it, take it, or plug it in — check.

Big Nope pulls three separate FDA recall feeds into one list per state, so you’re not searching three government databases to get one answer.

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/virusSalmonellaAnnounced 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/virusE. coliAnnounced 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)
UnclassifiedAllergenMilkUndeclaredAnnounced 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)
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)
UnclassifiedBacteria/virusSalmonellaE. coliAnnounced 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/virusSalmonellaAnnounced 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)

Recalls nationwide

Data last updated: September 9, 2026 at 1:18 PM UTC

19,422 recalls found
Wording
Class IHigh risk
FoodBacteria/virusListeriaRecalled March 20, 2017

Italian sub, 12". Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2090-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusListeriaRecalled March 20, 2017

Italian Sub, Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2089-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusListeriaRecalled March 20, 2017

Ham and Turkey 12" sub. Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2091-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusListeriaRecalled March 20, 2017

Turkey and Havarti sandwiches. Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2086-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusListeriaRecalled March 20, 2017

Turkey wedge sandwich. Prepared by Gourmet Classic Salads 240 E Bullard Ave. Lake Wales, FL 33853

FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.

Full report

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

Recall #:
F-2085-2017
Lot/product code:
Manufactured between 01/30/2017-02/22/2017, with expiration date through 03/01/2017.
Recalling firm:
Gourmet Classic Salads, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 12, 2017

EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS: Epipen Auto-Injector Jr. 0.15 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.

Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication

ALL 50 STATES
Full report

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

Recall #:
D-0691-2017
Lot/product code:
US lot 5GN767, expiration April 2017; lot 5GN773, expiration April 2017; lot 6GN215, expiration Sep 2017: INTERNATIONAL lot 5GR765, expiration March 2017; lot 5GK771, expiration April 2017; lot 5ED824, expiration April 2017; and lot 6ED117, expiration ***
Recalling firm:
Meridian Medical Technologies a Pfizer Company
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 12, 2017

EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS ---- Epipen Auto-Injector 0.3 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.

Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication

ALL 50 STATES
Full report

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

Recall #:
D-0690-2017
Lot/product code:
US: lot 5GM631, exp. April 2017; lot 5GM640, exp. May 2017; lot 6GM072, exp. Sep 2017; lot 6GM082, exp. Sep 2017; lot 6GM088, exp. Oct 2017; lot 6GM087, exp. Oct 2017; lot 6GM198, exp. Oct 2017; lot 6GM081, exp. Sep 2017; lot 6GM091, exp. Oct 2017; lot 6GM199, exp. Oct 2017: INTERNATIONAL: lot 5FA665, exp. April 2017; lot 5GU763, exp. May 2017; lot 6FA293, exp. Oct 2017; lot 6FA292, exp. Oct 2017; lot 6GH294, exp. Oct 2017.
Recalling firm:
Meridian Medical Technologies a Pfizer Company
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusE. coliRecalled March 9, 2017

Portion cup of soynut butter served with other food items such as milk, yogurt, raisins, and gold fish crackers, labeled and served on tray. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,

Possible contamination with E. coli O157

Full report

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

Recall #:
F-1952-2017
Lot/product code:
Product Code 8743. No expiration date
Recalling firm:
Greater Miami Caterers, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusE. coliRecalled March 9, 2017

Soynut Butter repackaged into smaller containers and labeled. Container amounts vary according to how servings are needed per order. Each serving size is 0.56 oz.. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,

Possible contamination with E. coli O157

Full report

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

Recall #:
F-1953-2017
Lot/product code:
Product Code 8458. No expiration date
Recalling firm:
Greater Miami Caterers, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusE. coliRecalled March 9, 2017

Half Wheat sandwich with soynut butter spread and jelly, served on tray. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,

Possible contamination with E. coli O157

Full report

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

Recall #:
F-1950-2017
Lot/product code:
Product Code 8464. No expiration date
Recalling firm:
Greater Miami Caterers, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusE. coliRecalled March 9, 2017

Whole Wheat sandwich with soynut butter spread and jelly, served on tray. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,

Possible contamination with E. coli O157

Full report

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

Recall #:
F-1951-2017
Lot/product code:
Product Code 8465. No expiration date
Recalling firm:
Greater Miami Caterers, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusE. coliRecalled March 9, 2017

Pan Pita with soynut butter spread on top, 4" pita. Manufactured by Greater Miami Caterers 4001 NW 31 Ave.,

Possible contamination with E. coli O157

Full report

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

Recall #:
F-1949-2017
Lot/product code:
Product Code 8491. No expiration date
Recalling firm:
Greater Miami Caterers, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenMilkUndeclaredRecalled February 24, 2017

7-Eleven, Mantecada MUFFIN, Net Wt. 4 oz. , UPC 05254859241-7, in clear flexible plastic, Distributed by 7-Eleven, Inc., Irving, TX 750634.

Not listed on the label Allergen: Milk

Full report

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

Recall #:
F-1912-2017
Lot/product code:
UPC 05254859241-7, SKU #9841
Recalling firm:
Bak EZ
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusListeriaRecalled 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
FoodBacteria/virusListeriaRecalled 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
FoodBacteria/virusListeriaRecalled February 4, 2017

Hot Pepper Cheese packaged as: (a) AMISH CLASSICS Hot Pepper RW Square, Item 26244, 12 lbs, UPC 858653262442 (b) Deli Made EZ Hot Pepper St Pk .5oz, Item 26555, 1.5 lbs, UPC 828653265559 (c) Deli Readi Hot Pepper St Pk 1oz Slice, Item 26831, 2 lbs, UPC 634660628788 (d) LIPARI Old Tyme Hot Pepper Cheese Food EW Square, Item 26703, 8 oz, UPC 94776102280

Potential cross contamination from a sample 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-1697-2017
Lot/product code:
Lot Numbers: (a) Best if Used by: 6/10/2017 (b) Best if Used by: 3/17/2017, 4/22/2017 (c) Best if Used by: 2/28/2017, 4/22/2017, 5/16/2017 (d) Best if Used by: 6/10/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusListeriaRecalled 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
FoodBacteria/virusListeriaRecalled 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
FoodBacteria/virusListeriaRecalled 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
FoodBacteria/virusListeriaRecalled 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
FoodBacteria/virusListeriaRecalled February 4, 2017

Jalapeno Cheese packaged as: (a) Deli Readi Jalapeno St Pk 1oz Slice, Item 10831, 2 lbs, UPC 634660628788

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-1709-2017
Lot/product code:
Lot Numbers: (a) 2/28/2017, 4/22/2017, 5/18/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusListeriaRecalled 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
FoodBacteria/virusListeriaRecalled 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
FoodBacteria/virusListeriaRecalled 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
FoodBacteria/virusListeriaRecalled 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)