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. 2,820 recalls have been distributed to New Jersey in the last 12 months.
Showing 7821–7840 of 29,496 recalls
Recalled Item: Torq-Flex Wire Guide Australian Modification Recalled by Cook Incorporated...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner PC Hydrophilic Wire Guide Recalled by Cook Incorporated Due to...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner PC Wire Guide (The Firm) Recalled by Cook Incorporated Due to...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bentson Wire Guide (20cm Distal Flexibility with Softened Tip) Recalled by...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lunderquist -Ring Torque Wire Guide Recalled by Cook Incorporated Due to...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Movable Core Wire Guide (Tefcor) Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bentson Wire Guide Recalled by Cook Incorporated Due to Cook Medical...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coons Interventional Wire Guide Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Movable Core Wire Guide (Tapered Tefcor) (OUS ONLY) Recalled by Cook...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner PC Wire Guide (Nimble Floppy) Recalled by Cook Incorporated Due...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixed Core Wire Guide (Straight) Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Panels CHOL+GLU Test Strips () Recalled by Polymer Technology Systems,...
The Issue: Incorrect instructions for use were packaged into the final product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner PC Wire Guide (Nimble) Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cope Mandril Wire Guide (Nitinol) Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to Hip liner...
The Issue: Hip liner implant boxes may contain knee inserts and knee insert boxes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWER 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to Hip...
The Issue: Hip liner implant boxes may contain knee inserts and knee insert boxes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humidifier bottle and syringe filter kit (6 count of each) Recalled by...
The Issue: There is a potential breach to the sterile barrier containing the Humidifier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humidifier bottle and syringe filter kit (6 count of each) Recalled by...
The Issue: There is a potential breach to the sterile barrier containing the Humidifier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...
The Issue: An out of specification component preventing the blue retention ring from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...
The Issue: An out of specification component preventing the blue retention ring from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.