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. 2,769 recalls have been distributed to New Jersey in the last 12 months.
Showing 14621–14640 of 53,621 recalls
Recalled Item: SAFE-T PLUS LUMBAR PUNCTURE TRAY ADULT Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE DRUG FREE TRAY 22G Recalled by Bard Peripheral Vascular Inc...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY ADULT 18G X 3.5 Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G Recalled by Bard Peripheral...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T PLUS LUMBARPUNCTURE TRAY ADULT Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL Recalled by Bard Peripheral...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray Recalled by Bard...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCA 4000 Curing Units Recalled by Envisiontec US Llc Due to The PCA 4000 may...
The Issue: The PCA 4000 may not fully cure EnvisionTEC dental resins to desired product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azacitidine Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed stability specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azacitidine Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed stability specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bortezomib Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed stability specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Steamable by Lidl Chopped Spinach NET WT 12 OZ (340 Recalled by Frozen Food...
The Issue: Possible contamination of Listeria monocytogenes in frozen chopped spinach.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dr. Snack Goji Berry Recalled by B.C.S. International Corporation Due to...
The Issue: Product contains undeclared sulfites.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SyncVision Systems Recalled by Volcano Corporation Due to If FFR...
The Issue: If FFR measurement(s) are made prior to an iFR/FFR co-registration/pullback...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Ultrasound System Recalled by Siemens Medical Solutions USA, Inc....
The Issue: The clip store function in the ultrasound imaging system does not work when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10...
The Issue: Failed Dissolution Specification: Dissolution results are below...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LINQ II Insertable Cardiac Monitor Recalled by Medtronic Inc., Cardiac...
The Issue: Devices may lose functionality due to susceptibility to moisture ingress.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions...
The Issue: individual components have been labelled with incorrect colours. The red and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.