FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Lamb Weston Sales
- Product
- Item SP204, Sprouts Organic Hash Browns Shredded Potatoes, 1…
- Reason
- Potential to be contaminated with Listeria monocytogenes.
- Published
- October 5, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Lamb Weston Sales
- Product
- Item GV020, Great Value Shredded Hash Browns, 4 lbs. bag, 6/…
- Reason
- Potential to be contaminated with Listeria monocytogenes.
- Published
- October 5, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Lamb Weston Sales
- Product
- Item AX058, Alexia Organic Seasoned Hashed Browns Yukon Sele…
- Reason
- Potential to be contaminated with Listeria monocytogenes.
- Published
- October 5, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Keswick Creamery at Carrock Farms LLC
- Product
- Vermeer Cheese in 4 oz to 12 oz packages
- Reason
- All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.
- Published
- October 5, 2022
- Distribution
- Distributed to farm stores and farmers m…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Keswick Creamery at Carrock Farms LLC
- Product
- Pasteurized milk cheese "Quark", multiple flavors "Dill and…
- Reason
- All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.
- Published
- October 5, 2022
- Distribution
- Distributed to farm stores and farmers m…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Keswick Creamery at Carrock Farms LLC
- Product
- Bovre, multiple flavors: plain; oregano and garlic; herbes d…
- Reason
- All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.
- Published
- October 5, 2022
- Distribution
- Distributed to farm stores and farmers m…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Keswick Creamery at Carrock Farms LLC
- Product
- Pasteurized milk cheese "Havarti" 4 oz to 12 oz packages
- Reason
- All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.
- Published
- October 5, 2022
- Distribution
- Distributed to farm stores and farmers m…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Keswick Creamery at Carrock Farms LLC
- Product
- Pasteurized milk cheese "Whole Milk Ricotta" 8 oz and 16 oz…
- Reason
- All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.
- Published
- October 5, 2022
- Distribution
- Distributed to farm stores and farmers m…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Keswick Creamery at Carrock Farms LLC
- Product
- Aged raw milk cheese "Feta" in 4 oz to 12 oz packages
- Reason
- All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.
- Published
- October 5, 2022
- Distribution
- Distributed to farm stores and farmers m…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Keswick Creamery at Carrock Farms LLC
- Product
- Aged raw milk cheese "Calverley" 4 oz to 12 oz packages
- Reason
- All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.
- Published
- October 5, 2022
- Distribution
- Distributed to farm stores and farmers m…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Keswick Creamery at Carrock Farms LLC
- Product
- Aged raw milk cheese "Wallaby" 4 oz to 12 oz packages
- Reason
- All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.
- Published
- October 5, 2022
- Distribution
- Distributed to farm stores and farmers m…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Keswick Creamery at Carrock Farms LLC
- Product
- Aged raw milk cheese "Vulkwin's Folly Scratch 2" 4oz-12oz pa…
- Reason
- All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.
- Published
- October 5, 2022
- Distribution
- Distributed to farm stores and farmers m…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Keswick Creamery at Carrock Farms LLC
- Product
- Aged raw milk cheese "Ploughman Cider Wash Tomme" batch 47 4…
- Reason
- All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.
- Published
- October 5, 2022
- Distribution
- Distributed to farm stores and farmers m…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Beverage Distribution Center Incorporated, LLC. (BDCI)
- Product
- "A&W Root Beer Zero Sugar" packaged in 20oz PET bottles. UPC…
- Reason
- Product contains undeclared sugar. Full sugar root beer was packaged in bottles labeled "sugar free"
- Published
- October 5, 2022
- Distribution
- Distributed in Washington DC, MD, PA, an…
View recall →
FDA Recall
Terminated
Historical recordClass III
Clonidine Hydrochloride Tablets, USP, 0.3 mg, 100-count bottle, Rx Only, Manufactured by: UNICHEM LABORATORIES LTD. Pilerne Ind. Estate, Pilerne, Bardez, Goa 403 511, India Manufactured for: UNICHEM PHARMACEUTICALS (USA), INC. East Brunswick, NJ 08816. NDC# 29300-137-01
by UNICHEM PHARMACEUTICALS USA INC
- Reason
- Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a 100-count bottle of 0.3 mg strength Clonidine Hydrochloride Tablets,
- Published
- September 28, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
Pepsico Inc
- Product
- Mountain Dew Major Melon Zero, 12 FL OZ (355mL) can, sold as…
- Reason
- The outer wraps match the liquid in the can (Zero Sugar - Mountain Dew Major Melon) however the primary package (can) is incorrect (Full Sugar Mountain Dew Major Melon). Product inside can matches the product/nutritional panel on the point-of-sale outer container wrap.
- Published
- September 28, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass I
PROPOFOL Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL glass fliptop vial (NDC 0409-4699-54) further packaged in a tray of 10 vials (NDC Carton: 0409-4699-24), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA
by Pfizer Inc.
- Reason
- Presence of particulate matter
- Published
- September 21, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product), 15 mg, Rx Only, 100 tablets per bottle, Teva Pharmaceuticals USA, Inc. North Wales, PA 19454, NDC 0555-0777-02.
by Teva Pharmaceuticals USA Inc
- Reason
- Labeling: Label Error on Declared Strength; A sealed 100-count bottle labeled with 15 mg actually contained 100 tablets of 20 mg strength of the drug product.
- Published
- September 21, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Synergy Hand Sanitizer, Non-Sterile Solution to help reduce bacteria that can potentially cause disease, For use when soap and water are not available, Alcohol 80% Topical Solution, Antiseptic, 8.5 oz./ 250 mL bottles, Made and Distributed by: Superior Glove Works Ltd., 36 Vimy Street, Acton, Ontario, L7J 1S1, Canada, Made in Canada, UPC: 779406201594.
by SUPERIOR GLOVE WORKS, LTD.
- Reason
- CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity and the Sum of All Impurities, above specification limits.
- Published
- September 21, 2022
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Lisinopril Tablets USP, 10 mg, 1000-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by: Lupin Limited, Nagpur- 441 108, India. NDC 68180-980-03
by Lupin Pharmaceuticals Inc.
- Reason
- Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.
- Published
- September 21, 2022
- Distribution
- Nationwide
View recall →
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
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