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. 1,858 recalls have been distributed to New Jersey in the last 12 months.
Showing 33921–33940 of 53,621 recalls
Recalled Item: Jalapeno Popper ASI. Product Code: T3934. 33 lb bags Recalled by All...
The Issue: Products have been recalled due to potential for Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Non-GMO Sour Cream & Onion / Deep River Snacks. Product Code: T3527. 50 lb...
The Issue: Products have been recalled due to potential for Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Buttermilk Ranch Snack Seasoning / Meat Chips. Product Code: T3760. 50 lb...
The Issue: Products have been recalled due to potential for Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DIAMONDBACK 360 Peripheral 1.50 Classic Recalled by Cardiovascular Systems...
The Issue: CSI discovered that a 1.50mm Solid Crown OAD was labeled as a 1.50mm Crown OED.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Integral Shaft & Stem 15x27 HA Coated Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Fixed Hinge Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Shaft L=120mm Recalled by Stanmore Implants Worldwide Ltd. Due to...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DF Coated Integral Shaft & Stem 15x30x38 Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medacta International SA Recalled by Medacta Usa Inc Due to Damaged...
The Issue: Damaged packaging, lack of sterility assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Metal Cased Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novacort Gel Sample Packets (2% hydrocortisone acetate Recalled by Novum...
The Issue: Subpotent Drug: Out of specification result for pramoxine hydrochloride
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT...
The Issue: A breach in the sterile packaging may have occurred resulting in potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT Recalled by...
The Issue: A breach in the sterile packaging may have occurred resulting in potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Robotic Radiosurgery Systems Recalled by Accuray Incorporated Due...
The Issue: Accuray has become aware of a potential safety issue involving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 10 cm 5 pack Product Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse Treatment Planning System version 13.MR2 [13.06.31 with Smart...
The Issue: Modifications in version 13.6MR2 for Contouring, SmartAdapt, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Section - BAR5490IVC Recalled by Invacare Corporation Due to A quality...
The Issue: A quality issue with the junction box used in the bariatric bed junction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment...
The Issue: Reunion TSA Peg Alignment Sound broke during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.