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Recalls affecting Georgia

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

17,406 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)
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High riskLow riskAll
Wording
Class IHigh risk
DrugChemicalUndeclaredRecalled June 18, 2020

A Clean Choice CBD, Hemp Oil Extract Tincture, French Vanilla, 1000 mg, 1 fl oz (30 ml) bottles, Made in Michigan for A Clean Choice, A Division of A Clean Cigarette, Inc., 3055 Bay Road Suite 1, Saginaw, MI 48603

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
▸Full report

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

Recall #:
D-1454-2020
Lot/product code:
FG003106
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalUndeclaredRecalled June 18, 2020

Tasty Drops, Hemp Oil Extract, Vanilla, 1500MG CBD,1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29086 6

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
▸Full report

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

Recall #:
D-1477-2020
Lot/product code:
FG003144, FG003249
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalUndeclaredRecalled June 18, 2020

Tasty Drops Hemp Oil Extract, Natural, 1 FL. OZ (30ML) bottles, 500mg CBD, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29084 2

Chemical Contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
▸Full report

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

Recall #:
D-1447-2020
Lot/product code:
FG003138 and FG003248
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalUndeclaredRecalled June 18, 2020

SP, hemp oil, Berry, 300MG CBD,1 FL. OZ (30 ML) bottles, Distributed by: The Spiffy Piff

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
▸Full report

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

Recall #:
D-1465-2020
Lot/product code:
FG003277
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalUndeclaredRecalled June 18, 2020

Tasty Drops Hemp Oil Extract, Vanilla, 1 FL. OZ (30ML) bottles, 300MG CBD, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 8 02991 76471 4

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
▸Full report

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

Recall #:
D-1450-2020
Lot/product code:
FG003126
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalUndeclaredRecalled June 18, 2020

BC Hemp Co., Full Spectrum Hemp Extract, CBD Oil, Spearmint, 500mg CBD, 1 FL. OZ (30 ML) bottles, Distributed by: B.C. Hemp Co., LLC, P.O. Box 156, Eau Claire, MI 49111

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
▸Full report

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

Recall #:
D-1459-2020
Lot/product code:
FG003315
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalUndeclaredRecalled June 18, 2020

Goodness Gurus, Healthy Hemp Drops Full Strength, 1000 MG/Spearmint, 1 FL. OZ bottles, Distributed by: Goodness Gurus, Inc., Carlisle, PA, UPC 53341 99311 3

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
▸Full report

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

Recall #:
D-1480-2020
Lot/product code:
FG003238
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalUndeclaredRecalled June 18, 2020

Made by Hemp 1000MG Hemp Extract, French Vanilla, 1 OZ (30 ML) bottles, Dist by: MHR Brands, Jenison, MI, UPC 8 02991 76553 7

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
▸Full report

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

Recall #:
D-1451-2020
Lot/product code:
FG003107
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
FoodUndeclaredRecalled May 27, 2019

"DEEP***GOLDEN RAISINS***NET WT***198g/7oz***DEEP FOODS, INC. UNION, NJ 07083"

Deep Foods Inc., 1090 Springfield Road, Union, NJ-07083 is initiating a recall of Deep Golden Raisins because of not listed on the label sulfites.

ALL 50 STATES
▸Full report

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

Recall #:
F-1981-2019
Lot/product code:
This recall covers 7oz, 14oz, and 28oz sizes with the following UPC codes: 7oz: 011433133432 14oz: 011433133449 28oz: 011433433457
Recalling firm:
Deep Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 26, 2019

MONARCH SOUTHERN BARBECUE SAUCE MADE WITH MUSTARD NET 128 FL OZ(1 GAL) 3.78L INGREDIENTS: WATER, HIGH FRUTOSE CORN SRYUP, SUGAR, TOMATO PASTE, DISTILLED AND CIDER VINEGAR, SALT ***DISTRIBUTED BY/DISTRIBUIDO POR US FOODS, INC., ROSEMOUNT, IL 60015 UPC 7 58108 60016 4

Monarch Southern BBQ contains soy and wheat. The firm had labels that properly described the product as Monarch Southern BBQ, but did not have the correct UPC, nutrition panel, ingredient statement or allergen declaration.

FLGANCSCTNVA
▸Full report

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

Recall #:
F-1303-2019
Lot/product code:
Product Item number 06678, Lot numbers18352M, 19015M, 19016M, 19030M, 19043M
Recalling firm:
The CF Sauer Company
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled October 5, 2018

LADYFINGERS GOURMET TO GO SIGNATURE SHAVED COUNTRY HAM ROLLS; ONE DOZEN PER PACKAGE (15oz - 425 grams); ALLERGEN INFORMATION: CONTAINS WHEAT, PRODUCED IN FACILITY THAT PROCESSES PEANUTS AND TREE NUTS. www.ladyfingersofraleigh.com; 919-828-2270; 627 East Whitaker Mill Rd Raleigh, NC 27608; UPC 8 56149 00509 9.

The firm was notified by their vendor that the product may be contaminated with Listeria monocytogenes.

CADCDEGANCNYSCVA
▸Full report

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

Recall #:
F-0065-2019
Lot/product code:
All product on the market.
Recalling firm:
Ladyfingers Catering, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled October 4, 2018

Callie's Charleston Biscuits COCKTAIL HAM BISCUITS; 24 NET WT. 35 OZ (980 g) Callie's Charleston Biscuits; 1895 Avenue F, Charleston, SC 18405 843 577.1198; CALLIESBISCUITS.COM

The firm was notified by one of their vendors that the ham used in their product may be contaminated with Listeria monocytogenes

AKALARAZCACOCTDCDEFLGAHIIAIDILINKSKYLAMAMDMEMIMNMOMSMTNCNDNENHNJNMNVOHOKORPARISCSDTNTXUTVAVTWAWIWVWY
▸Full report

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

Recall #:
F-0066-2019
Lot/product code:
050417, 060617, 060717, 080117, 091917, 092717, 110617, 120417, 121617, 070619, 080819, 101019, 102319, 110119, 111419, 122119 & 010920.
Recalling firm:
Callie's Charleston Biscuits
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled October 4, 2018

Callie's Charleston Biscuits COUTRY HAM BISCUITS; 18 NET WT. 18 OZ (510 g) Callie's Charleston Biscuits; 1895 Avenue F, Charleston, SC 18405 843 577.1198; CALLIESBISCUITS.COM

The firm was notified by one of their vendors that the ham used in their product may be contaminated with Listeria monocytogenes

AKALARAZCACOCTDCDEFLGAHIIAIDILINKSKYLAMAMDMEMIMNMOMSMTNCNDNENHNJNMNVOHOKORPARISCSDTNTXUTVAVTWAWIWVWY
▸Full report

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

Recall #:
F-0067-2019
Lot/product code:
050417, 052417, 053017, 071017, 072417, 080117, 081417, 082217, 091417, 092717, 101017, 101117, 102417, 110617, 110817, 111417, 112017, 113017, 120817, 121117, 121417, 121817, 122217, 070219, 071519, 081319, 082619, 090819, 091519, 092619, 092719, 101019, 101619, 102319, 110119, 111119, 111419, 112919, 121319, 122119, 010920, 013020, 020620 & 031920.
Recalling firm:
Callie's Charleston Biscuits
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 15, 2018

Montelukast Sodium Tablets 10 mg, 30-count bottle, Rx Only, By: Hetero Hetero Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar - 509 301, India, Manfuactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, NDC 31722-726-30

Labeling: Label Mix-Up - One lot labeled Montelukast Sodium Tablets 10 mg tablets may contain 90 tablets of Losartan Potassium 50 mg.

ALL 50 STATES
▸Full report

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

Recall #:
D-0081-2019
Lot/product code:
Lot #: MON17384, Exp 12/19
Recalling firm:
Hetero Labs Limited Unit V
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled April 27, 2018

Vans gluten free Original 6 WAFFLES NET WT 9 OZ (255g) INGREDIENTS:***VAN'S GLUTEN FREE MIX (BROWN RICE FLOUR, POTATO STARCH, RICE FLOUR, SOY FLOUR),***RICE FLOUR,***SUNFLOWER AND/OR SOY LECITHIN***CONTAINS: SOY DISTRIBUTED BY: VAN'S INTERNATIONAL FOODS SAN DIEGO, CA 92154 UPC 0 89947 30206 4

The firm was notified that they failed to include the allergens milk & wheat in their ingredient statement.

ARCACOGAILMINJNYPATXWI
▸Full report

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

Recall #:
F-1475-2018
Lot/product code:
Lot Code #A640234710 WL2, BEST BY AUG 22, 2018
Recalling firm:
Tyson Foods Discovery Center
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled April 19, 2018

Happy Harvest Leaf Spinach; Net Wt. 13.5 oz (383g); Ingredients: Spinach, Water, Salt. Distributed by Aldi Inc. Batavia, IL 60510; Product of USA; Manufactured In A Facility That Processes Peanuts and Soy. May Contain Peanuts and Soy. Packaged in a steel 2-piece can.

Canned spinach is being recalled due to the potential to contain boiled peanuts instead of spinach.

FLGAIAILINKYMIMNNCOHSCSDTNVAWIWV
▸Full report

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

Recall #:
F-1412-2018
Lot/product code:
Lot Code: SPIN71A23IX Use by January 2021; UPC: 041498131289
Recalling firm:
Mccall Farms Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled April 13, 2018

Shell Eggs packaged in quantities and styles of pack (plastic and pulp cartons, flats, and boxes)

Shell eggs have the potential to be contaminated with Salmonella Braenderup.

ALCTFLGAMDMSNCNHNJNYSCUTVA
▸Full report

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

Recall #:
F-1410-2018
Lot/product code:
Plant Number P-1065; LOT CODES with a Julian date ranged from 011 - 102; Numerous UPCs
Recalling firm:
ROSE ACRE FARM
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled March 6, 2018

Maurice's Honey Southern Gold BBQ Sauce; Net Wt. 18 oz. bottles; UPC Code 0 7561654332 6 and Carolina Gold Honey Sauce; Net Wt. 18 oz. bottle; UPC Code 0 7561654383 8

Not listed on the label soy and wheat ingredients

ALL 50 STATES
▸Full report

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

Recall #:
F-0978-2018
Lot/product code:
All lots
Recalling firm:
Piggie Park Enterprises Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled April 21, 2017

Infant 25% DEXTROSE Injection, USP, 2.5 g (250 mg/mL), 10 mL Unit of Use Single-dose Syringe per carton, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-1775-10

Presence of Particulate Matter: human hair found within an internal sample syringe.

ALL 50 STATES
▸Full report

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

Recall #:
D-0862-2017
Lot/product code:
Lot 58382EV*, Exp 1OCT 2017, *lot may be followed by 01 or 02
Recalling firm:
Hospira Inc.
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
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
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

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

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

FLGAILINKSKYMAMIMOOHPASCTNTXUT
▸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/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

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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)