FoodDec 7, 2016
Mel-O Cream Donuts International Jumbo Pershing recall — FDA F-0540-2017
Human fingertip found in product filling line.
Class IIFDA: TerminatedMel-O Cream Donuts International, Inc.
Latest records
Latest recalls — page 1752
The newest recall records with useful source details are listed here.
FoodDec 7, 2016
Mel-O Cream Donuts International Hy Vee Shells recall — FDA F-0548-2017
Human fingertip found in product filling line.
Class IIFDA: TerminatedMel-O Cream Donuts International, Inc.
FoodDec 7, 2016
Kuster's A New Dairy Pepper Jack cut Cheese, 5 lb recall — FDA F-0443-2017
Kuster's, Inc. is voluntarily recalling its shredded, sliced and cubed cheese following a supplier's recall of cheese due to the potential for the cheese to be contaminated with Listeria…
Class IFDA: TerminatedKuster's Inc.
FoodDec 7, 2016
Mel-O Cream Donuts International Arrowhead/Christmas Tree Shells recall — FDA F-0541-2017
Human fingertip found in product filling line.
Class IIFDA: TerminatedMel-O Cream Donuts International, Inc.
FoodDec 7, 2016
Kuster's 5 lb recall — FDA F-0442-2017
Kuster's, Inc. is voluntarily recalling its shredded, sliced and cubed cheese following a supplier's recall of cheese due to the potential for the cheese to be contaminated with Listeria…
Class IFDA: TerminatedKuster's Inc.
FoodDec 7, 2016
Kuster's Nor-Tech Dairy Sharp White Cheddar Feather Shred Cheese, 5 lb recall — FDA F-0440-2017
Kuster's, Inc. is voluntarily recalling its shredded, sliced and cubed cheese following a supplier's recall of cheese due to the potential for the cheese to be contaminated with Listeria…
Class IFDA: TerminatedKuster's Inc.
FoodDec 7, 2016
Mel-O Cream Donuts International Hy Vee Long Shells recall — FDA F-0547-2017
Human fingertip found in product filling line.
Class IIFDA: TerminatedMel-O Cream Donuts International, Inc.
FoodDec 7, 2016
Benson's Old Home Kitchens Bakery Division Old Home Kitchens, 14 oz recall — FDA F-0533-2017
Undeclared allergen; Peanut Protein
Class IIFDA: TerminatedBenson's Old Home Kitchens Bakery Division
FoodDec 7, 2016
Kuster's Fata's Best PepperJack Feather Shred Shredded Cheese, 5 lb recall — FDA F-0438-2017
Kuster's, Inc. is voluntarily recalling its shredded, sliced and cubed cheese following a supplier's recall of cheese due to the potential for the cheese to be contaminated with Listeria…
Class IFDA: TerminatedKuster's Inc.
FoodDec 7, 2016
Mel-O Cream Donuts International Star Shaped Shells recall — FDA F-0542-2017
Human fingertip found in product filling line.
Class IIFDA: TerminatedMel-O Cream Donuts International, Inc.
DrugDec 7, 2016
Burel Pharmaceuticals UROLET MB URINARY ANTISEPTIC, ANTISPASMODIC Tablets, Each tablet recall — FDA D-0156-2017
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Class IIFDA: TerminatedBurel Pharmaceuticals Inc.
DrugDec 7, 2016
Nationwide Laboratories Salsalate Tablets, USP, 750 mg recall — FDA D-0166-2017
CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.
Class IIFDA: TerminatedNationwide Laboratories, LLC
DrugDec 7, 2016
Burel Pharmaceuticals UROPHEN MB URINARY ANTISEPTIC Tablets, Each tablet contains recall — FDA D-0158-2017
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Class IIFDA: TerminatedBurel Pharmaceuticals Inc.
DrugDec 7, 2016
Metformin Hydrochloride Tablets, USP 500 mg, 1000 tablets recall — FDA D-0163-2017
Presence of Foreign Tablets/Capsules; report of Amlodipine Tablets found in 1000 count bottles of Metformin Hydrochloride Tablets USP
Class IIFDA: TerminatedAscend Laboratories LLC
DrugDec 7, 2016
Nationwide Laboratories Salsalate Tablets, USP, 500 mg recall — FDA D-0165-2017
CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.
Class IIFDA: TerminatedNationwide Laboratories, LLC
DrugDec 7, 2016
Burel Pharmaceuticals Indiomin MB URINARY ANTISEPTIC, ANTISPASMODIC Capsules, Each capsule recall — FDA D-0160-2017
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Class IIFDA: TerminatedBurel Pharmaceuticals Inc.
DrugDec 7, 2016
Burel Pharmaceuticals Hyolev MB URINARY ANTISEPTIC Tablets, Each tablet for oral recall — FDA D-0155-2017
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Class IIFDA: TerminatedBurel Pharmaceuticals Inc.
DrugDec 7, 2016
Cadila Pharmaceuticals Ondansetron HCI API, Bulk, Manufacturer: Cadila Pharmaceuticals recall — FDA D-0164-2017
Microbial Contamination of Non-Sterile Product
Class IIFDA: TerminatedCadila Pharmaceuticals Limited
DrugDec 7, 2016
Burel Pharmaceuticals URAMIT MB URINARY ANTISEPTIC Capsules, Each capsule contains recall — FDA D-0157-2017
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Class IIFDA: TerminatedBurel Pharmaceuticals Inc.
DrugDec 7, 2016
Nationwide Laboratories Phenazopyridine Hydrochloride Tablets, USP, 100 mg, 100 count recall — FDA D-0167-2017
CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.
Class IIFDA: TerminatedNationwide Laboratories, LLC
DrugDec 7, 2016
Burel Pharmaceuticals AZUPHEN MB URINARY ANTISEPTIC Capsules, Each capsule contains recall — FDA D-0159-2017
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
Class IIFDA: TerminatedBurel Pharmaceuticals Inc.
DrugDec 7, 2016
Par Pharmaceutical Travoprost Ophthalmic Solution USP, 0.004%, a) 2.5 mL and b) 5 mL bottles recall — FDA D-0154-2017
Lack of Assurance of Sterility; damage to the internal portion of the dropper tip portion of the container
Class IIFDA: TerminatedPar Pharmaceutical, Inc.
DrugDec 7, 2016
Nationwide Laboratories Phenazopyridine Hydrochloride Tablets, USP, 200 mg, 100 count recall — FDA D-0168-2017
CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.
Class IIFDA: TerminatedNationwide Laboratories, LLC
Medical DeviceNov 30, 2016
Depuy Orthopaedics ACTIS Flex Reamers SZ 0/1 recall — FDA Z-0650-2017
DePuy Orthopaedics, Inc. is issuing a voluntary recall for all lots of the ACTIS Flex Reamers due to the instruments breaking and potentially leaving pieces in the patient.
Class IIFDA: TerminatedDepuy Orthopaedics Inc.
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