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. 2,642 recalls have been distributed to New Jersey in the last 12 months.
Showing 28561–28580 of 53,621 recalls
Recalled Item: Intera 0.5T Standard Recalled by Philips Electronics North America...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conversion SmarthPath to dStream for 1.5T Recalled by Philips Electronics...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T: 1) Nova (Dual) Recalled by Philips Electronics North America...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T10-NT Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama 1.0T Recalled by Philips Electronics North America Corporation Due...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Lunar: a) DPX NT Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Lunar: a) DPX Duo Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.0T Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns TCM Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Update to cooler-heater cleaning instructions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo HX2 Temperature Management System Recalled by Terumo Cardiovascular...
The Issue: Update to cooler-heater cleaning instructions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5 Model 78104 Product Usage: Indicated for use as a Recalled by Philips...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare: a) Prodigy Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All Alka-Seltzer Plus¿ packages with a full front panel instant Recalled by...
The Issue: Labeling: Label Mix-Up: Bayer is recalling all Alka-Seltzer Plus packages,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by InvaGen Pharmaceuticals,...
The Issue: Failed Dissolution Specifications; during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by InvaGen Pharmaceuticals,...
The Issue: Failed Dissolution Specifications; during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: URO-3 Triple Stain (CD44 + p53) with CK20 Recalled by Biocare Medical, LLC...
The Issue: Immunohistochemistry device kits found to display incorrect staining pattern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.