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. 2,603 recalls have been distributed to New Jersey in the last 12 months.
Showing 38181–38200 of 53,621 recalls
Recalled Item: Dark Chocolate Recalled by Cape Cod Provisions LLC Due to Undeclared Almonds
The Issue: Product may contain undeclared almonds
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bearded Brothers BOLD Coconut Curry Net Wt. 1.5 oz/43 g . Recalled by...
The Issue: Mold on energy bars.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bearded Brothers BOLD The Greek Net Wt. 1.5 oz/43 g . Recalled by Bearded...
The Issue: Mold on energy bars.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cervical Spine Locking Plate (CSLP) System Recalled by Synthes (USA)...
The Issue: DePuy Synthes is initiating a Voluntary Medical Device Recall of lot #...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Lumen Pressure Monitoring Sets and Trays The subject sets Recalled by...
The Issue: A manufacturing process may lead to catheter tip fracture and or separation....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Artery Pressure Monitoring Catheter Sets and Trays The subject...
The Issue: A manufacturing process may lead to catheter tip fracture and or separation....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Lumen Central Venous Catheter Sets and Trays The subject Recalled by...
The Issue: A manufacturing process may lead to catheter tip fracture and or separation....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Pressure Monitoring Catheter Sets and Trays The subject...
The Issue: A manufacturing process may lead to catheter tip fracture and or separation....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.