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. 2,696 recalls have been distributed to New Jersey in the last 12 months.
Showing 19781–19800 of 29,496 recalls
Recalled Item: IMMULITE/IMMULITE 1000 Systems Prostate-Specific Antigen (PSA) Assay...
The Issue: Siemens Healthcare Diagnostics has confirmed that the IMMULITE/ IMMULITE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ddR Formula B X-ray System Recalled by Swissray Medical Due to Potential for...
The Issue: Potential for bucky (the part that holds the grid and is moveable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco TRP System The Monaco system is used to make Recalled by Elekta, Inc....
The Issue: Contours are not handled correctly if the CT dataset contains slices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraSeal XT Plus Clear . The package contains 4x 1.2 Recalled by Ultradent...
The Issue: There was a labeling error with product, UltraSeal XT Plus Clear , Part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (R) DEAD BLOW MALLET Recalled by Smith & Nephew, Inc. Due to The firm...
The Issue: The firm received complaints of cracks in the weld on the head of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightMix¿ Zika rRT-PCR Test The LightMix¿ Zika rRT-PCR Test is Recalled by...
The Issue: The LightCycler¿ 480 algorithm used for the LightMix¿ Zika rRT-PCR Test, EUA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affinity Fusion" Oxygenator with Integrated Arterial Filter Recalled by...
The Issue: Medtronic is initiating a voluntary product recall for specific lot numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck Facial Closure Systems have application in laparoscopic procedures for...
The Issue: The devices wings may become partially detached from the EFx Shield during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM)...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS System Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge System Recalled by Siemens Medical Solutions USA,...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash System Recalled by Siemens Medical Solutions USA,...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empowr Knee System Product Usage: Non-porous proximal tibial baseplate...
The Issue: A size 4 Empowr baseplate was mislabeled as a size 6. The affected lot was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 728321 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT 728326 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 728232 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 728323 Recalled by Philips Medical Systems (Cleveland)...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 728231 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.