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. 2,874 recalls have been distributed to New Jersey in the last 12 months.
Showing 381–400 of 29,496 recalls
Recalled Item: Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X. Product Code (REF): (1) 781358 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with Recalled...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for XR and 3.0T. Product Code (REF): Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X. Product Code (REF): (1) 781356 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S. Product Code (REF): (1) 781357 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade to MR 7700. Product Code (REF): 782130. MR systems Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T. Product Code (REF): (1) 781341 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and...
The Issue: Complaints received that Vanta A71200 CP App does not function as intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter...
The Issue: Boston Scientific is initiating the removal of certain batches of Coyote"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis ES Enterprise Server Catalog Numbers 1115-00 Recalled by CareFusion...
The Issue: Due a software issue that may result in equipment not receiving timely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...
The Issue: Affected implants may have undersized distal diameter along length of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...
The Issue: Affected implants may have undersized distal diameter along length of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...
The Issue: Affected implants may have undersized distal diameter along length of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK 2-Pack Recalled by Microbiologics Inc Due to Affected units may...
The Issue: Affected units may fail to recover the target microorganism Campylobacter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...
The Issue: Affected implants may have undersized distal diameter along length of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...
The Issue: Affected implants may have undersized distal diameter along length of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...
The Issue: Affected implants may have undersized distal diameter along length of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...
The Issue: Affected implants may have undersized distal diameter along length of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...
The Issue: Affected implants may have undersized distal diameter along length of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.