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. 2,653 recalls have been distributed to New Jersey in the last 12 months.
Showing 26181–26200 of 53,621 recalls
Recalled Item: ACCOLADE Pacemaker Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESSENTIO Pacemaker Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model 3300 LATITUDE(TM) Programming System Product Usage - The Boston...
The Issue: There is a potential for the Pacing System Analyzer (PSA) to exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VISIONIST X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker) Recalled by...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Delivers 0.1 mg/day...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: V-Twin Recalled by Vital Scientific N.V. Due to The action is being...
The Issue: The action is being initiated because the cooling indicator board was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APS Accelerator modular systems Recalled by Abbott Laboratories, Inc Due to...
The Issue: The firm identified customer sites where modules which the safety pacemaker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...
The Issue: There is lot to lot variability for QC and patient results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...
The Issue: There is lot to lot variability for QC and patient results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codan Filter (Codan catalog number BC 693) used with Medrad Recalled by...
The Issue: Bayer has received reports of loose particulate in the filter when the dust...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bupropion Hydrochloride ER Tablets Recalled by InvaGen Pharmaceuticals, Inc....
The Issue: Failed impurities/ degradation specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP 50 mL Viaflex container Baxter Recalled...
The Issue: cGMP Deviation
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole dihydrochloride extended release tablets Recalled by Par...
The Issue: Failed impurities/degradation specifications: Finished product contain a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Implant Direct Scan Adapter Assembly Replant platform for the following...
The Issue: The action is being initiated due to incorrect assembly of the scan adapter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II blood return warmer for Prismaflex Product...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.