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. 2,862 recalls have been distributed to New Jersey in the last 12 months.
Showing 2561–2580 of 29,496 recalls
Recalled Item: 3M Unitek Transbond Plus Self-Etching Primer (100 unit Recalled by 3M Unitek...
The Issue: Due to an increase of complaints for bracket bond failures and skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number:...
The Issue: Potential for procedural delays or interruptions during use of the Auryon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...
The Issue: Telemetry receiver systems may experience a Windows proxy Issue causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code Recalled...
The Issue: Due to complaints received for the marker band detaching from the distal tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 9mm - Silicone Recalled by Adept...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 6mm - Double - Silicone Recalled by...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - Donaldson - Blue Silicone Recalled by Adept...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 9mm - Double - Silicone Recalled by...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 12mm - Silicone Recalled by Adept...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.