FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
HELLOFRESH US
- Product
- HelloFresh Meal Kit Product Code 2-3-8-10-15-18-19-22-23 fro…
- Reason
- Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
- Published
- November 24, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
HELLOFRESH US
- Product
- HelloFresh Meal Kit Product Code 2-5-8-9-16-19-21-22-23-24-2…
- Reason
- Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
- Published
- November 24, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
HELLOFRESH US
- Product
- HelloFresh Meal Kit Product Code 2-7-17-19-21-25-AB from Pro…
- Reason
- Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
- Published
- November 24, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
KEELER FAMILY FARMS
- Product
- Whole raw onions - YELLOW - imported from Chihuahua, Mexico…
- Reason
- Potential contamination with Salmonella Oranienburg in onions from Chihuahua, Mexico.
- Published
- November 24, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
KEELER FAMILY FARMS
- Product
- Whole raw onions - WHITE - imported from Chihuahua, Mexico a…
- Reason
- Potential contamination with Salmonella Oranienburg in onions from Chihuahua, Mexico.
- Published
- November 24, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
KEELER FAMILY FARMS
- Product
- Whole raw onions - RED - imported from Chihuahua, Mexico and…
- Reason
- Potential contamination with Salmonella Oranienburg in onions from Chihuahua, Mexico.
- Published
- November 24, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Seneca Foods Corporation
- Product
- Sliced Pickled Beets, Net Wt 16oz. (1lb) 454g, packaged unde…
- Reason
- Lack of acidulant.
- Published
- November 24, 2021
- Distribution
- Multiple states
View recall →
FDA Recall
Terminated
Historical recordClass II
Tadalafil Tablets, USP 20 mg, 30 count bottle, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Limited, India, NDC # 16714-077-01
by SUN PHARMACEUTICAL INDUSTRIES INC
- Reason
- Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.
- Published
- November 17, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Tadalafil Tablets, USP 5 mg, 30 count bottle, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Limited, India, NDC # 16714-075-01
by SUN PHARMACEUTICAL INDUSTRIES INC
- Reason
- Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.
- Published
- November 17, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Ezetimibe and Simvastatin Tablets, 10 mg/80mg, 500 tablet bottles, Rx only, Manufactured by Dr. Reddy's Laboratories LA LLC Shreveport, LA 71106 USA, Packaged by GSMS, Incorporated Camarillo, CA 93012 USA; NDC 51407-193-05
by Golden State Medical Supply Inc.
- Reason
- Failed Excipient Specification; product manufactured using an excipient found to be OOS for conductivity
- Published
- November 17, 2021
- Distribution
- Distributed to two distributors located…
View recall →
FDA Recall
Terminated
Historical recordClass II
Acetaminophen Oral Suspension, 325 mg/10.15 mL, packaged in 10.15 mL per cup (NDC Individual cup: 68094-330-59), in a) 30-count case (NDC 30-count case: 68094-330-62), and b) 100-count case (NDC 100-count case: 68094-330-61), Hospital Use Only, Pkg. Precision Dose, Inc., S. Beloit, IL 61080.
by Precision Dose Inc.
- Reason
- cGMP Deviations: Product manufactured with contaminated raw ingredient.
- Published
- November 17, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Acetaminophen Oral Suspension, 160 mg/5 mL, packaged in 5 mL per cup (NDC Individual cup: 68094-231-59), in a) 30-count case (NDC 30-count case: 68094-231-62), and b) 100-count case (NDC 100-count case: 68094-231-61), Hospital Use Only, Pkg. Precision Dose, Inc., S. Beloit, IL 61080.
by Precision Dose Inc.
- Reason
- cGMP Deviations: Product manufactured with contaminated raw ingredient.
- Published
- November 17, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Cefixime Capsules 400 mg, 50 capsules bottles, Rx Only, Manufactured by: Alken Laboratories Ltd., Mumbai - 400 013, India, Distributed by: Ascend Laboratories LLC, Parsippany, NJ, 07054 NDC 67877-584-50
by Ascend Laboratories LLC
- Reason
- Failed Impurities/Degradation Specifications
- Published
- November 17, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Ezetimibe and Simvastatin Tablets, 10 mg/40mg, a) 90 Tablets, b) 500 tablets, Rx only, Manufactured by Dr. Reddy's Laboratories LA LLC Shreveport, LA 71106 USA, Packaged by GSMS, Incorporated Camarillo, CA 93012 USA; NDC: a) 51407-192-90, b) 51407-192-05
by Golden State Medical Supply Inc.
- Reason
- Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin Tablets, 10 mg/10 mg were found in the bottle
- Published
- November 17, 2021
- Distribution
- Distributed to two distributors located…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Simply Delicious, Inc.
- Product
- Bobo's Almond Butter Protein Bar, 2.2 oz., 4-pack Multipack,…
- Reason
- Almond Butter Bars contain undeclared peanuts.
- Published
- November 17, 2021
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
NOW Health Group Inc.
- Product
- NOW Bee Pollen 500mg 100 VCAPS UPC 733739025203
- Reason
- Product may contain Metronidazole
- Published
- November 17, 2021
- Distribution
- Total number of domestic consignees = 15…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
NOW Health Group Inc.
- Product
- NOW Ginseng & Royal Jelly 90 VCAPS UPC 733739040077 MMA Nutr…
- Reason
- Product may contain Metronidazole
- Published
- November 17, 2021
- Distribution
- Total number of domestic consignees = 15…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
NOW Health Group Inc.
- Product
- NOW Royal Jelly 1500mg 60 VCAPS UPC 733739025654 NOW Royal…
- Reason
- Product may contain Metronidazole
- Published
- November 17, 2021
- Distribution
- Total number of domestic consignees = 15…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
The Kroger Co
- Product
- Country Oven Party Balloon Cake 48oz
- Reason
- Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
- Published
- November 17, 2021
- Distribution
- Product distributed to the following sta…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
The Kroger Co
- Product
- Country Oven Raspberry Cake 71oz
- Reason
- Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
- Published
- November 17, 2021
- Distribution
- Product distributed to the following sta…
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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