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. 1,024 recalls have been distributed to New Jersey in the last 12 months.
Showing 32121–32140 of 53,621 recalls
Recalled Item: B85996 Recalled by Newly Weds Foods Inc Due to Undeclared Milk
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: A27980 Recalled by Newly Weds Foods Inc Due to Undeclared Milk
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: B52547 Recalled by Newly Weds Foods Inc Due to Undeclared Milk
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: A98404 Recalled by Newly Weds Foods Inc Due to Undeclared Milk
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: B57511 Recalled by Newly Weds Foods Inc Due to Undeclared Milk
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: A96231 Recalled by Newly Weds Foods Inc Due to Undeclared Milk
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: B52609 Recalled by Newly Weds Foods Inc Due to Undeclared Milk
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: A58602 Recalled by Newly Weds Foods Inc Due to Undeclared Milk
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OptiLite Multi-Use Holmium Laser Fibers Recalled by Cook Inc. Due to Cook...
The Issue: Cook Inc. is initiating a voluntary recall of the OptiLite Multi-Use Holmium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Best Practice Kit Recalled by Medtronic Due to Potential for an incomplete...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures. BIOSYN: BIOSYN 4/0 18" VIOLET CV-25 DT Recalled by Medtronic Due to...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USPACK-SUTURE KIT Recalled by Medtronic Due to Potential for an incomplete...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures. POLYSORB: POLSORB 0 18 U/D PRECUT 126R Recalled by Medtronic Due to...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSTOM SUTURE PACK Recalled by Medtronic Due to Potential for an incomplete...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures. MAXON: MAXON 4/0 5X18" GREEN CV-24 D-TACH Recalled by Medtronic Due...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCHRITTMACHER ANGIO X3 Recalled by Medtronic Due to Potential for an...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures. ENDO STITCH: ENDO STITCH POLYSORB 0 48" U/D DLU SU Recalled by...
The Issue: Potential for an incomplete seal on the inner package, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620 A1 Recalled by GE Healthcare, LLC Due to Carestation 620,...
The Issue: Carestation 620, 650 and 650c has Potential for Elevated FiCO2 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD Recalled by...
The Issue: Implant Direct Sybron Manufacturing is recalling the Legacy Full-Contour...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 70 Ultrasound System Intended for use by trained personnel (doctor...
The Issue: The strength of the arm mounting mechanism was insufficient and had to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.