Product Recalls in New Jersey
Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,632 recalls have been distributed to New Jersey in the last 12 months.
Showing 34801–34820 of 53,621 recalls
Recalled Item: Pressure Monitoring Kit (MeriTrans"). Catalog Number K11-00232G Recalled by...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manifold Kit. Catalog Number K09-11867AP Recalled by Merit Medical Systems,...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V. Mueller Neuro/Spine Recalled by Cardinal Health 200, LLC Due to Potential...
The Issue: Potential risk associated with corrosion demonstrated on the distraction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluid Management Set. Catalog Number K08-MP5159A Recalled by Merit Medical...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Brivo 715 Prime Recalled by GE OEC Medical Systems, Inc Due to GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC Brivo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product...
The Issue: There is a potential for a component failure of the device which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Navigation O-arm O2 Surgical Imaging System Product Catalog...
The Issue: O-arm O2 Surgical Imaging System Spatial calibration may be erroneous in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBRA Fusion 50 Ablation System Recalled by AtriCure, Inc. Due to Due to...
The Issue: Due to product design and process control, part of the device can separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PARICALCITOL Capsules Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PARICALCITOL Capsules Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PARICALCITOL Capsules Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIKAJI Chowpati BHELPURI Recalled by KRISHNA FOOD CORP Due to Potential...
The Issue: FDA sample analysis revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cookies Bergen Recalled by Dollar General Corporation Due to Mold found in...
The Issue: Mold found in cookie product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CD79b PE (ASR) Recalled by Becton, Dickinson and Company, BD Biosciences Due...
The Issue: CD79b (SN8) PE is contaminated with a FITC conjugate of unknown antigenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carnitine-L 250 mg/mL Injectable Recalled by Wells Pharmacy Network LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trimix Injectable 30 mg/1 mg/10 mcg/mL a) 2 mL and b) 5 mL and c) 10 mL...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glutamine/ORNI/ARGIN/LYSINE/LIDO Injectable Recalled by Wells Pharmacy...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mitomycin Solution Injectable Recalled by Wells Pharmacy Network LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sermorelin Acetate/GHRP (2) & (6) 9 mg/9 mg/9 mg Injectable Kit Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sermorelin Acetate/GHRP (2) 3 mg/4.5 mg Injectable Kit Recalled by Wells...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.