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 28921–28940 of 29,496 recalls
Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...
The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 volume imaging ultrasound systems at software versions VA16C...
The Issue: In some cases, the system is unable to capture a clip or image during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS FLEXIBLE ARTERIAL CANNULA: 8.0 MM (24 FR) WITH 3/8" CONNECTOR Recalled...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-COATED TRANSPLANT PACK Product Usage: The Sarns Cardioplegia Cannula and...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS HIGH-FLOW AORTIC ARCH CANNULA: 6.5 MM (20 FR) 00 WITH 3/8" CONNECTOR...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS FLEXIBLE ARTERIAL CANNULA: 8.0 MM (24 FR) 00 WITH 3/8" CONNECTOR...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS HIGH-FLOW AORTIC ARCH CANNULA: 6.5 MM (20 FR) 00 WITH 3/8" CONNECTOR...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPECIALTYCARE - HUDGENS. The Sarns High Flow Aortic Arch Cannula Recalled by...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FX PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS ANTEGRADE CARDIOPLEGIA CANNULA: ROOT INFUSION CANNULA WITH 12-GAUGE...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INDIANA/OHIO HEART Product Usage: The Sarns Cardioplegia Cannula and...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.