FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Mondelez Global Llc
- Product
- 40Z NAB CLASSIC VPACK SC, 120CT MOD 40 Oz Carton 6 Ritz Bi…
- Reason
- Mondelez Global received notification from a supplier, Associated Milk Producers, Inc. ( AMPI ), of a voluntary recall of Whey Powder Sweet Type as a precautionary measure due to the potential presence of Salmonella. The recalled whey powder is used as an ingredient in various Mondelez Global human food products.
- Published
- August 8, 2018
- Distribution
- The impacted products were shipped to Co…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Mondelez Global Llc
- Product
- 1Z RITZ BITS CHEESE 120 1 Oz Pouches
- Reason
- Mondelez Global received notification from a supplier, Associated Milk Producers, Inc. ( AMPI ), of a voluntary recall of Whey Powder Sweet Type as a precautionary measure due to the potential presence of Salmonella. The recalled whey powder is used as an ingredient in various Mondelez Global human food products.
- Published
- August 8, 2018
- Distribution
- The impacted products were shipped to Co…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Mondelez Global Llc
- Product
- 20Z NAB CKIES CLASSIC MULTI PK 4 20 Oz, Carton, 5 Ritz Bit…
- Reason
- Mondelez Global received notification from a supplier, Associated Milk Producers, Inc. ( AMPI ), of a voluntary recall of Whey Powder Sweet Type as a precautionary measure due to the potential presence of Salmonella. The recalled whey powder is used as an ingredient in various Mondelez Global human food products.
- Published
- August 8, 2018
- Distribution
- The impacted products were shipped to Co…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Mondelez Global Llc
- Product
- 4/12Z RBS CHEESE MULTI PK, 12 Oz Carton 4 cartons per case
- Reason
- Mondelez Global received notification from a supplier, Associated Milk Producers, Inc. ( AMPI ), of a voluntary recall of Whey Powder Sweet Type as a precautionary measure due to the potential presence of Salmonella. The recalled whey powder is used as an ingredient in various Mondelez Global human food products.
- Published
- August 8, 2018
- Distribution
- The impacted products were shipped to Co…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Mondelez Global Llc
- Product
- RITZ BITS CHEESE BIG BAG 3Z 3 OZ, Pouch, 12 per case
- Reason
- Mondelez Global received notification from a supplier, Associated Milk Producers, Inc. ( AMPI ), of a voluntary recall of Whey Powder Sweet Type as a precautionary measure due to the potential presence of Salmonella. The recalled whey powder is used as an ingredient in various Mondelez Global human food products.
- Published
- August 8, 2018
- Distribution
- The impacted products were shipped to Co…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Mondelez Global Llc
- Product
- 10.8Z RITZ SANDWICH WITH CHEESE 14 (2 & 13) 10.8 Oz per tra…
- Reason
- Mondelez Global received notification from a supplier, Associated Milk Producers, Inc. ( AMPI ), of a voluntary recall of Whey Powder Sweet Type as a precautionary measure due to the potential presence of Salmonella. The recalled whey powder is used as an ingredient in various Mondelez Global human food products.
- Published
- August 8, 2018
- Distribution
- The impacted products were shipped to Co…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Mondelez Global Llc
- Product
- RITZ BITS CHEESE BIG BAG 3 Oz, Pouch Retail: 12 per case F…
- Reason
- Mondelez Global received notification from a supplier, Associated Milk Producers, Inc. ( AMPI ), of a voluntary recall of Whey Powder Sweet Type as a precautionary measure due to the potential presence of Salmonella. The recalled whey powder is used as an ingredient in various Mondelez Global human food products.
- Published
- August 8, 2018
- Distribution
- The impacted products were shipped to Co…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
LL'S MAGNETIC CLAY INC
- Product
- Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastro…
- Reason
- The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts.
- Published
- August 8, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Enalapril Maleate, USP 5MG, 30-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0693-30
by Aidarex Pharmaceuticals LLC
- Reason
- Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.
- Published
- August 1, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Enalapril Maleate, USP 5MG, 90-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0693-90
by Aidarex Pharmaceuticals LLC
- Reason
- Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.
- Published
- August 1, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Enalapril Maleate, USP 2.5MG, 90-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0977-90
by Aidarex Pharmaceuticals LLC
- Reason
- Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.
- Published
- August 1, 2018
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Valsartan Tablets, USP 320 mg, 90-count bottle (NDC 0591-2170-19), 500-count bottle (NDC 0591-2170-05), Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054.
by Teva Pharmaceuticals USA
- Reason
- CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
- Published
- August 1, 2018
- Distribution
- Product was distributed throughout the U…
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FDA Recall
Ongoing
Historical recordClass II
Valsartan Tablets, USP 160 mg, 90-count bottle (NDC 0591-2169-19), 1000-count bottle (NDC 0591-2169-10), Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054
by Teva Pharmaceuticals USA
- Reason
- CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
- Published
- August 1, 2018
- Distribution
- Product was distributed throughout the U…
View recall →
FDA Recall
Ongoing
Historical recordClass II
Valsartan Tablets, USP 80 mg, 90-count bottle (NDC 0591-2168-19), 1000-count bottle (NDC 0591-2168-10), Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054
by Teva Pharmaceuticals USA
- Reason
- CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
- Published
- August 1, 2018
- Distribution
- Product was distributed throughout the U…
View recall →
FDA Recall
Ongoing
Historical recordClass II
Valsartan Tablets, USP 40 mg, 30-count bottle (NDC 0591-2167-30), 90-count bottle (NDC 0591-2167-19), Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054
by Teva Pharmaceuticals USA
- Reason
- CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
- Published
- August 1, 2018
- Distribution
- Product was distributed throughout the U…
View recall →
FDA Recall
Ongoing
Historical recordClass II
Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 320 mg/25 mg tablets, USP, 90-count bottle, Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054. NDC 0591-2318-19.
by Teva Pharmaceuticals USA
- Reason
- CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
- Published
- August 1, 2018
- Distribution
- Product was distributed throughout the U…
View recall →
FDA Recall
Ongoing
Historical recordClass II
Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 320 mg/12.5 mg tablets, USP, 90-count bottle, Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054. NDC 0591-2318-19
by Teva Pharmaceuticals USA
- Reason
- CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
- Published
- August 1, 2018
- Distribution
- Product was distributed throughout the U…
View recall →
FDA Recall
Ongoing
Historical recordClass II
Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 160 mg/25 mg tablets, USP 90-count bottle, Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054. NDC 0591-2317-19.
by Teva Pharmaceuticals USA
- Reason
- CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
- Published
- August 1, 2018
- Distribution
- Product was distributed throughout the U…
View recall →
FDA Recall
Ongoing
Historical recordClass II
Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 160 mg/12.5 mg tablets, USP 90-count bottle, Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054. NDC 0591-2316-19.
by Teva Pharmaceuticals USA
- Reason
- CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
- Published
- August 1, 2018
- Distribution
- Product was distributed throughout the U…
View recall →
FDA Recall
Ongoing
Historical recordClass II
Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 80 mg/12.5 mg tablets, 90 count-count bottle, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054, NDC 0591-2315-19.
by Teva Pharmaceuticals USA
- Reason
- CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
- Published
- August 1, 2018
- Distribution
- Product was distributed throughout the U…
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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