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 20021–20040 of 29,496 recalls
Recalled Item: MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S61CM D66CM GLOBAL...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 10F C90¿ S79CM D84CM Catalog # AB101078 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alligator Retrieval Device The device is intended for use in Recalled by...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C55¿ S61CM D66CM Catalog # AB081040 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C90¿ S61CM D66CM Catalog # AB081042 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN SMN 10699533 (500 test)...
The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C120¿ S61CM D66CM Catalog # AB081043 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C90¿ S79CM D84CM Catalog # AB081046 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 10F STRAIGHT S61CM D66CM Catalog # AB10218 Recalled...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accessory Adapter Part number 600525A0 Product Usage: designed for the...
The Issue: Maquet Inc. is initiating a voluntary field action on the Accessory Adapter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C120¿ S79CM D84CM Catalog # AB081047 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marathon Flow Directed Micro Catheter Recalled by Micro Therapeutics Inc,...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C55¿ S79CM D84CM Catalog # AB081044 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C55¿ S79CM D84CM GLOBAL...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C70¿ S79CM D84CM Catalog # AB081045 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZWAY 10F STRAIGHT S79CM D84CM Catalog # AB101219 Recalled...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S79CM D84CM GLOBAL...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C70¿ S61CM D66CM GLOBAL...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Antibacterial Hydrophilic Intermittent Catheter Recalled by C.R....
The Issue: Misbranding; the product labeled as an Antibacterial Hydrophilic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C70¿ S61CM D66CM Catalog # AB081041 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.