FoodNov 18, 2020
Meijer Inc./Traffic Dept 40oz Clear plastic container, UPC 219210112216 recall — FDA F-0104-2021
potential risk of Salmonella
Class IFDA: TerminatedMeijer Inc./Traffic Dept.
Latest records
Latest recalls — page 938
The newest recall records with useful source details are listed here.
FoodNov 18, 2020
WOLFGANG CONFECTIONERS Hu Cashew Hunks, Hu Cashews + Vanilla Bean Chocolate Covered recall — FDA F-0095-2021
Wolfgang Confectioners, 50 E. 4th Avenue, York, PA 17404, has initiated a recall of Hu Almond Hunks and Hu Cashew Hunks, in 4 oz., stand up pouch, 6 bags per case because of mislabeled…
Class IIFDA: TerminatedWOLFGANG CONFECTIONERS
FoodNov 18, 2020
B&G Foods Back to Nature Organic Rosemary & Olive Oil Stoneground Wheat recall — FDA F-0123-2021
B&G Foods initiated a recall of Back to Nature Organic Rosemary & Olive Oil Stoneground Wheat Crackers, 6 oz. with a best by date of APR 25 2021, because package may be filled with peanut…
Class IFDA: TerminatedB&G Foods North America, Inc.
FoodNov 18, 2020
Starwest Botanicals Elderberry Whole Organic recall — FDA F-0114-2021
Direct customer tested product upon receipt and had a positive result for Salmonella.
Class IIFDA: TerminatedStarwest Botanicals, Inc.
DrugNov 18, 2020
H & H Remedies Union (black) salve recall — FDA D-0071-2021
CGMP Deviations
Class IIFDA: TerminatedH & H Remedies, LLC
DrugNov 18, 2020
Baxter Healthcare Bupivacaine Hydrochloride in 8.25% Dextrose Injection, USP Spinal 0.75% recall — FDA D-0076-2021
Presence of particulate matter in solution - black and transparent particles
Class IIFDA: TerminatedBaxter Healthcare Corporation
DrugNov 18, 2020
H & H Remedies White Liniment recall — FDA D-0072-2021
CGMP Deviations
Class IIFDA: TerminatedH & H Remedies, LLC
DrugNov 18, 2020
Mesalamine Delayed-Release Tablets, USP 1.2 gram, 120 tablets per bottle recall — FDA D-0069-2021
Failed Dissolution Specifications: Out-of-specification dissolution results were obtained during stability testing.
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugNov 18, 2020
H & H Remedies Vapor Ointment recall — FDA D-0073-2021
CGMP Deviations
Class IIFDA: TerminatedH & H Remedies, LLC
VehicleNov 18, 2020
Volkswagen Group of camera recall — NHTSA campaign 20V716000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021 Atlas Cross Sport, Tiguan LWB, Jetta NF, Jetta GLI, Golf GTI, Atlas FL and Arteon vehicles. The rear view camera…
cameraVolkswagen Group of America, Inc.
VehicleNov 17, 2020
Model Y control arm recall — NHTSA campaign 20V709000
Tesla, Inc. (Tesla) is recalling certain 2020 Model Y vehicles. The bolts connecting the front upper control arm and steering knuckle may have not been properly tightened, allowing the…
control armTesla, Inc.
VehicleNov 12, 2020
Jeep Grand Cherokee gas recirculation valve (egr valve) recall — NHTSA campaign 20V699000
Chrysler (FCA US LLC) is recalling certain 2014-2019 Jeep Grand Cherokee vehicles equipped with the 3.0L EcoDiesel engines. The Exhaust Gas Recirculation (EGR) cooler may crack and allow…
gas recirculation valve (egr valve)Chrysler (FCA US LLC)
Medical DeviceNov 11, 2020
Zimmer Biomet ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, 10 recall — FDA Z-0372-2021
Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for…
Class IIFDA: TerminatedZimmer Biomet, Inc.
Medical DeviceNov 11, 2020
3M Company - Health Care Business 3M Red Dot Monitoring Electrode with 4mm Adapter - Product recall — FDA Z-0421-2021
Corrosion could cause performance failures in the product.
Class IIFDA: Terminated3M Company - Health Care Business
Medical DeviceNov 11, 2020
Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of recall — FDA Z-0418-2021
5F Micro-Introducer Kits may not contain the correct device, packaged with a 4F Sheath/Dilator component
Class IIFDA: TerminatedAngiodynamics, Inc.
Medical DeviceNov 11, 2020
Synthes (USA) Products DePuy Synthes SYNMESH 10MM DIA 18MM HEIGHT (TI) Product Number recall — FDA Z-0403-2021
Incorrectly Labeled 'general medical device,' printed on the statutory label of the SYNMESH CAGE SYSTEM instead of 'specially controlled medical device"
Class IIIFDA: TerminatedSynthes (USA) Products LLC
Medical DeviceNov 11, 2020
GE Healthcare GE Datex-Ohmeda Aisys CS2 Anesthesia System - Product Usage: is intended to recall — FDA Z-0313-2021
Flow sensors could have damaged tubes in the form of small punctures or cuts.
Class IIFDA: OngoingGE Healthcare, LLC
Medical DeviceNov 11, 2020
Synthes (USA) Products STANDARD RING 22MM X 28MM (TI) Product Number: 495-406 - Product recall — FDA Z-0416-2021
Incorrectly Labeled 'general medical device,' printed on the statutory label of the SYNMESH CAGE SYSTEM instead of 'specially controlled medical device"
Class IIIFDA: TerminatedSynthes (USA) Products LLC
Medical DeviceNov 11, 2020
Synthes (USA) Products END RING 22MM X 28MM LATERAL OR ANTERIOR/0 DEG (TI) Product Number recall — FDA Z-0413-2021
Incorrectly Labeled 'general medical device,' printed on the statutory label of the SYNMESH CAGE SYSTEM instead of 'specially controlled medical device"
Class IIIFDA: TerminatedSynthes (USA) Products LLC
Medical DeviceNov 11, 2020
Synthes (USA) Products END RING 17MM X 22MM LATERAL OR ANTERIOR/0 DEG (TI) Product Number recall — FDA Z-0411-2021
Incorrectly Labeled 'general medical device,' printed on the statutory label of the SYNMESH CAGE SYSTEM instead of 'specially controlled medical device"
Class IIIFDA: TerminatedSynthes (USA) Products LLC
Medical DeviceNov 11, 2020
Zimmer Biomet ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm recall — FDA Z-0345-2021
Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for…
Class IIFDA: TerminatedZimmer Biomet, Inc.
Medical DeviceNov 11, 2020
Zimmer Biomet ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm recall — FDA Z-0347-2021
Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for…
Class IIFDA: TerminatedZimmer Biomet, Inc.
Medical DeviceNov 11, 2020
Zimmer Biomet ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm recall — FDA Z-0353-2021
Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for…
Class IIFDA: TerminatedZimmer Biomet, Inc.
Medical DeviceNov 11, 2020
Zimmer Biomet ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm recall — FDA Z-0354-2021
Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for…
Class IIFDA: TerminatedZimmer Biomet, Inc.
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