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. 2,642 recalls have been distributed to New Jersey in the last 12 months.
Showing 30641–30660 of 53,621 recalls
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corporation...
The Issue: Lack of Assurance of Sterility: Customer complaints for leaking bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fogarty Adherent Clot Catheter Model Numbers 1408010 and 140806 Product...
The Issue: The diameter of the Fogarty Catheter balloon, measures 6mm instead of 10mm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dial-A-Dose Insulin Delivery Device (Pen-Injector) cartridge holders Product...
The Issue: A small number of batches may crack or break if exposed to certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche / Hitachi MODULAR Analyzer Systems-Immunoassay...
The Issue: A software malfunction can occur on the cobas e 411 and Elecsys 2010...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol TC Reusable Electrodes (TCN) Recalled by Cosman Medical, LLC Due to...
The Issue: After multiple reprocessing cycles, the epoxy resin which holds the TCN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee System Recalled by Zimmer Biomet, Inc. Due to Finishing...
The Issue: Finishing guide does not adequately account for shape differences present in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phadia 1000 Instrument Recalled by Phadia US Inc Due to The "Retry" command...
The Issue: The "Retry" command does not function properly which could cause a shortage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600...
The Issue: Teleflex Medical is recalling the affected product because there may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e 411 Immunoassay Analyzer-Model/Catalog/Part number:...
The Issue: A software malfunction can occur on the cobas e 411 and Elecsys 2010...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anarkali Peshawari Naan Bread Frozen 15oz. retail plastic pouch 24 Recalled...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clif Builders Chocolate Mint 12-count Recalled by Clif Bar & Company Due to...
The Issue: Undeclared peanuts and/or tree nuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clif Kid Zbar Protein Chocolate Chip 10-pack Recalled by Clif Bar & Company...
The Issue: Undeclared peanuts and/or tree nuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clif Kid Zbar Protein Chocolate Mint 10-pack Recalled by Clif Bar & Company...
The Issue: Undeclared peanuts and/or tree nuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clif Builders Variety Pack Chocolate Peanut Butter and Chocolate Mint...
The Issue: Undeclared peanuts and/or tree nuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clif Kid Zbar Protein Variety Pack 30-count Recalled by Clif Bar & Company...
The Issue: Undeclared peanuts and/or tree nuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ULTRA-STEN Rapid Size and Strength capsules Recalled by HARDCORE...
The Issue: Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: D-ZINE Rapid Size and Strength capsules Recalled by HARDCORE FORMULATIONS...
The Issue: Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur Recalled...
The Issue: Three (3) complaints were identified in which the potential for utilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORA System with VerifEye+ Cart Recalled by Alcon Research, Ltd. Due to Some...
The Issue: Some ORA Carts have the potential to return an incorrect IOL power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.