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. 2,551 recalls have been distributed to New Jersey in the last 12 months.
Showing 46421–46440 of 53,621 recalls
Recalled Item: Pleo Not TABLETS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Recalled by McKesson Packaging Services Due to...
The Issue: Failed Dissolution Specification: Out of Specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...
The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...
The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Popsicle Orange Cherry Grape 20 pops Net 33 fl oz Unilever Englewood Cliffs...
The Issue: Unilever United States, Inc. is voluntarily recalling a limited number of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer Recalled by Roche...
The Issue: electrode used beyond the guaranteed in-use 52 week lifetime,may leak and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube...
The Issue: The product may fail to achieve seal of right lung due to the cuff inflating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound...
The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound...
The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. K102239...
The Issue: GE Healthcare has recently become aware of potential safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Activa RC (37612) Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic neurostimulators. Restore (37711) Recalled by Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10" Hemoglobin Testing System Recalled by Bio-Rad Laboratories, Inc. Due...
The Issue: On a rare occasion the D-10 software might generate an extra result by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort Slim Implantable Port Recalled by Bard Access Systems Due to...
The Issue: Labeling discrepancy.The label states that the implantable port contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hand Control 12FR Suction Coagulator with 10 ft cord and holster Recalled by...
The Issue: Megadyne Medical Products, Inc. is voluntarily recalling Hand Control 12Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advil PM Caplets Recalled by Pfizer Us Pharmaceutical Group Due to Subpotent...
The Issue: Subpotent Drug: This lot is being recalled because of out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Price Chopper Orange Juice Recalled by Dean Foods, Inc. Due to Undeclared Dairy
The Issue: undeclared dairy in orange juice
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lehigh Valley Dairy Farms Orange Juice FROM CONCENTRATE Recalled by Dean...
The Issue: undeclared dairy in orange juice
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lehigh Valley Dairy Farms Orange Juice from concentrate HALF PINT (236 mL)...
The Issue: undeclared dairy in orange juice
Recommended Action: Do not consume. Return to store for a refund or discard.