FoodNov 21, 2018
Maribel's Sweets Cacao Market by MarieBelle Orange Peels 60% Dark Chocolate recall — FDA F-0428-2019
Product contains undeclared milk.
Class IFDA: TerminatedMaribel's Sweets, Inc.
Latest records
Latest recalls — page 1320
The newest recall records with useful source details are listed here.
FoodNov 21, 2018
Ukrop's Homestyle Foods NET WT 11 OZ recall — FDA F-0613-2019
The products may have come into contact with equipment used to process the country ham the supplier recalled for Listeria monocytogenes.
Class IFDA: TerminatedUkrop's Homestyle Foods, LLC
FoodNov 21, 2018
Ukrop's Black Forest Ham & Provolone Sub NET WT 7.8 OZ recall — FDA F-0605-2019
The products may have come into contact with equipment used to process the country ham the supplier recalled for Listeria monocytogenes.
Class IFDA: TerminatedUkrop's Homestyle Foods, LLC
FoodNov 21, 2018
Ukrop's Homestyle Foods NET WT 5.5 OZ recall — FDA F-0614-2019
The products may have come into contact with equipment used to process the country ham the supplier recalled for Listeria monocytogenes.
Class IFDA: TerminatedUkrop's Homestyle Foods, LLC
FoodNov 21, 2018
Maribel's Sweets Cacao Market by MarieBelle Rosemary Truffle Salt 60% Dark recall — FDA F-0427-2019
Product contains undeclared milk.
Class IFDA: TerminatedMaribel's Sweets, Inc.
FoodNov 21, 2018
Ukrop's Homestyle Foods NET WT 14 OZ recall — FDA F-0606-2019
The products may have come into contact with equipment used to process the country ham the supplier recalled for Listeria monocytogenes.
Class IFDA: TerminatedUkrop's Homestyle Foods, LLC
FoodNov 21, 2018
Ukrop's Homestyle Foods NET WT 17.7 OZ recall — FDA F-0607-2019
The products may have come into contact with equipment used to process the country ham the supplier recalled for Listeria monocytogenes.
Class IFDA: TerminatedUkrop's Homestyle Foods, LLC
FoodNov 21, 2018
Ukrop's Homestyle Foods NET WT 8.3 OZ recall — FDA F-0609-2019
The products may have come into contact with equipment used to process the country ham the supplier recalled for Listeria monocytogenes.
Class IFDA: TerminatedUkrop's Homestyle Foods, LLC
DrugNov 21, 2018
Breckenridge Pharmaceutical Megestrol Acetate Oral Suspension, USP 625 mg/5mL, 150 mL bottle recall — FDA D-0279-2019
Failed Stability Specifications: Out-of-Specification results obtained for particle size distribution during stability testing.
Class IIIFDA: TerminatedBreckenridge Pharmaceutical, Inc.
DrugNov 21, 2018
Kadesh International puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc. recall — FDA D-0250-2019
Non-Sterility: Product manufactured under non-sterile production conditions.
Class IFDA: TerminatedKadesh International
DrugNov 21, 2018
Teva Pharmaceuticals USA Alprostadil Injection USP 500 micrograms/mL 1 mL single use vial, 5 recall — FDA D-0244-2019
Failed Impurities/Degradation Specifications; out-of-specification results for impurities obtained during routine stability testing
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugNov 21, 2018
AMITIZA (lubiprostone) capsules 8 mcg. 60-count bottle recall — FDA D-0286-2019
Failed Impurities/Degradation Specifications:Elevated levels of a known impurity in the 20-month stability sample testing.
Class IIIFDA: TerminatedTakeda Development Center Americas, Inc.
DrugNov 21, 2018
ERBITUX CETUXIMAB Injection, 200 mg/100 mL (2 mg/mL), 100 mL per single-use vial recall — FDA D-0248-2019
Labeling: Missing label; potential for missing primary container label on the vial.
Class IIIFDA: TerminatedEli Lilly & Co
DrugNov 21, 2018
Epic Products Euphoric Premium Male Performance Enhancer capsules recall — FDA D-0288-2019
Marketed Without An Approved NDA/ANDA: product contains undeclared sildenafil, tadalafil, and oxytetracycline, FDA approved drug products making Euphoric an unapproved drug.
Class IFDA: TerminatedEpic Products, LLC
DrugNov 21, 2018
Taro Pharmaceuticals U.S.A Children's 24 Hour Allergy (cetirizine hydrochloride) Oral recall — FDA D-0276-2019
Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
Class IIFDA: TerminatedTaro Pharmaceuticals U.S.A., Inc.
DrugNov 21, 2018
Taro Pharmaceuticals U.S.A children's allergy relief (cetirizine hydrochloride) oral recall — FDA D-0278-2019
Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
Class IIFDA: TerminatedTaro Pharmaceuticals U.S.A., Inc.
DrugNov 21, 2018
RemedyRepack Metoprolol Tartrate Injection, USP 5mg/5mL, vials recall — FDA D-0245-2019
Failed pH Specifications: High Out-of-Specification results for pH were obtained during stability testing.
Class IIIFDA: TerminatedRemedyRepack Inc.
DrugNov 21, 2018
CHILDRENS ALLERGY children's allergy (cetirizine hydrochloride) Oral Solution, 1 mg/mL recall — FDA D-0277-2019
Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
Class IIFDA: TerminatedTaro Pharmaceuticals U.S.A., Inc.
VehicleNov 20, 2018
Chrysler seats recall — NHTSA campaign 18V822000
Chrysler (FCA US LLC) is recalling certain 2019 RAM 1500 trucks. The seat track position sensor on the manually-adjusted passenger seats may come loose and out of position, preventing the…
seatsChrysler (FCA US LLC)
Medical DeviceNov 14, 2018
GE Healthcare Centricity Universal Viewer with PACS-IW foundation 6.0.x displays medical recall — FDA Z-0375-2019
Synchronization failure
Class IIFDA: TerminatedGE Healthcare, LLC
Medical DeviceNov 14, 2018
Randox Laboratories Liquid Cardiac Control, CQ5051 recall — FDA Z-0380-2019
Randox has previously issued a recall for Liquid Cardiac Control CQ5053 lot 4245CK under REC334 on June 8, 2018. The firm has now confirmed the Liquid Cardiac Controls CQ5051, CQ5052 and…
Class IIFDA: TerminatedRandox Laboratories Ltd.
Medical DeviceNov 14, 2018
Randox Laboratories Liquid Cardiac Control, CQ5052 recall — FDA Z-0381-2019
Randox has previously issued a recall for Liquid Cardiac Control CQ5053 lot 4245CK under REC334 on June 8, 2018. The firm has now confirmed the Liquid Cardiac Controls CQ5051, CQ5052 and…
Class IIFDA: TerminatedRandox Laboratories Ltd.
Medical DeviceNov 14, 2018
Becton Dickinson & Company PCEA ASV Yellow Microbore, Catalog Numbers 30893, 30893-07 recall — FDA Z-0386-2019
The products have the potential to leak between the connection of the male luer lock and the yellow striped tubing.
Class IIFDA: TerminatedBecton Dickinson & Company
Medical DeviceNov 14, 2018
Integrity Implants FlareHawk Interbody Fusion System recall — FDA Z-0405-2019
Recently Integrity Implants uncovered a discrepancy in the cleaning parameters in several of their labeling material. The firm is initiating the field correction to ensure that updated…
Class IIFDA: TerminatedIntegrity Implants Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
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