FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Tippin's Gourmet Pies, LLC
- Product
- Tippins 9" Keylime Base packaged in ?. UPC code is 68081600…
- Reason
- Product was manufactured with an ingredient which has the potential to contain low levels of peanut residue.
- Published
- September 7, 2016
- Distribution
- Recalled product was distributed to Kans…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Lactalis American Group, Inc.
- Product
- PRESIDENT brand Authentic Pub Cheese SPREADABLE CHEESE, Ched…
- Reason
- The product contains undeclared wheat from ingredient used in production.
- Published
- September 7, 2016
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Tippin's Gourmet Pies, LLC
- Product
- Tippins Mini Key Lime Base packaged in ?. UPC code is 68081…
- Reason
- Product was manufactured with an ingredient which has the potential to contain low levels of peanut residue.
- Published
- September 7, 2016
- Distribution
- Recalled product was distributed to Kans…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Tippin's Gourmet Pies, LLC
- Product
- Tippins 9" Cream Cheese Base packaged in ?. UPC code is 680…
- Reason
- Product was manufactured with an ingredient which has the potential to contain low levels of peanut residue.
- Published
- September 7, 2016
- Distribution
- Recalled product was distributed to Kans…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
International Foodsource, LLC
- Product
- Sam International Bulk Raw Whole Pistachio 80% VP Net Wt. 3…
- Reason
- Raw pistachios may be contaminated with Salmonella which was determined through FDA contract laboratory testing.
- Published
- September 7, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Tippin's Gourmet Pies, LLC
- Product
- Tippins 8" Key Lime Base packaged in ?. UPC code is 6808160…
- Reason
- Product was manufactured with an ingredient which has the potential to contain low levels of peanut residue.
- Published
- September 7, 2016
- Distribution
- Recalled product was distributed to Kans…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Pearson Foods Inc.
- Product
- Kale, 4/ 1 lb, & 1 /2 lb shredded packaged in plastic, keep…
- Reason
- Pearson Foods Corporation is voluntarily recalling a limited number of packaged Kale products because they may be contaminated with Salmonella.
- Published
- September 7, 2016
- Distribution
- Domestic Only: IL, MI, WI No Foreign…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
International Foodsource, LLC
- Product
- IFS Club Bag Pistachio Raw Shelled 80% Wholes Net Wt. 3 lb.…
- Reason
- Raw pistachios may be contaminated with Salmonella which was determined through FDA contract laboratory testing.
- Published
- September 7, 2016
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Hampton Creek Foods
- Product
- JUST Cinnamon Roll Coffee Cake Mix; NET WT 26.9 oz. (1 lb 1…
- Reason
- Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
- Published
- September 7, 2016
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Pearson Foods Inc.
- Product
- Nappa Shredded 2/5 lb, packaged in plastic, keep refrigerate…
- Reason
- Pearson Foods Corporation is voluntarily recalling a limited number of packaged Kale products because they may be contaminated with Salmonella.
- Published
- September 7, 2016
- Distribution
- Domestic Only: IL, MI, WI No Foreign…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
International Foodsource, LLC
- Product
- Valued Natural Raw Pistachio Kernels Net Wt 5 oz. (141 g) I…
- Reason
- Raw pistachios may be contaminated with Salmonella which was determined through FDA contract laboratory testing.
- Published
- September 7, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Hampton Creek Foods
- Product
- JUST White Cake Mix; NET WT 20 oz. (1 lb 4 oz) 567 g); UPC…
- Reason
- Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
- Published
- September 7, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Hampton Creek Foods
- Product
- JUST Devil's Food Cake Mix; NET WT 20 oz. (1 lb 4 oz) 567…
- Reason
- Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
- Published
- September 7, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Hydrocortisone and acetic acid otic solution, Rx only, 10 mL bottle, Distributed by Actavis Inc. 60 Columbia Road Bldg B. Morristown, NJ 07560 USA , NDC 45963-412-61
by Actavis Inc
- Reason
- Failed Impurities/Degradation Specifications: Out of specification (OOS) results for related compound G were obtained at 12-month (at expiry) stability time-point for room temperature sample(s).
- Published
- August 31, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Acetasol HC (hydrocortisone and acetic acid otic solution USP) , Rx Only, 10 mL bottle, Manufactured by: Actavis Midatlantic LLC 1877 Kawai Road Lincolnton, NJ 28092 USA, NDC 0472-0882-82
by Actavis Inc
- Reason
- Failed Impurities/Degradation Specifications: Out of specification (OOS) results for related compound G were obtained at 12-month (at expiry) stability time-point for room temperature sample(s).
- Published
- August 31, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Amoxicillin for Oral Suspension USP, 400 mg/ 5 mL, 50 mL bottle, Rx only, Manufactured In Canada by: Teva Canada Limited, Toronto, Canada, NDC 0093-4161-76
by Teva North America
- Reason
- Superpotent drug: Out of specification test result for assay during stability testing.
- Published
- August 31, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Desoximetasone Gel USP, 0.05%, packaged in 60 gram aluminum tubes, Rx only, Marketed by: VersaPharm Incorporated Marietta, GA 30062, Manufactured by: Ei LLC Kannapolis, NC 28083, NDC 61748-205-60.
by Akorn, Inc.
- Reason
- Failed impurities/degradation specifications: product was out of specification for unknown impurity at the 9 month stability time point
- Published
- August 31, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Amlodipine Besylate Tablets, USP, 10 mg*, packaged in a) 100-count (10 x 10) unit dose blisters per carton, NDC 51079-452-20; b) 300-count (10 x 30) unit dose blisters per carton, NDC 51079-452-56; and c) 25-count (25 x 1) Robot-Rx Ready Packages in a carton, NDC 51079-452-19; Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505; Packaged and Distributed By: UDL Laboratories, Inc., Rockford, IL 61103.
by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)
- Reason
- CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.
- Published
- August 31, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Amlodipine Besylate Tablets, USP, 5 mg*, packaged in a) 100-count (10 x 10) unit dose blisters per carton, NDC 51079-451-20; b) 300-count (10 x 30) unit dose blisters per carton, NDC 51079-451-56, c) 25-count (25 x 1) Robot-Rx Ready Packages in a carton, NDC 51079-451-19; and d) 30-count tablets per dosage card in a carton, NDC 51079-451-69, Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505; Packaged and Distributed By: UDL Laboratories, Inc., Rockford, IL 61103.
by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)
- Reason
- CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.
- Published
- August 31, 2016
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Amlodipine Besylate Tablets, USP, 2.5 mg*, packaged in a)100-count (10 x 10) unit dose blisters per carton, NDC 51079-450-20 and b) 30-count tablets per dosage card in a carton, NDC 51079-450-63, Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505; Packaged and Distributed By: UDL Laboratories, Inc., Rockford, IL 61103.
by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)
- Reason
- CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.
- Published
- August 31, 2016
- 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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