Product Recalls in North Carolina
Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,042 recalls have been distributed to North Carolina in the last 12 months.
Showing 18321–18340 of 54,363 recalls
Recalled Item: IceSphere" 1.5 CX 90¿ Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed" 1.5 90¿ Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceRod" 1.5 i-Thaw" Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed" 1.5 MRI Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MH-200S Recalled by Shimadzu Medical Systems Due to The firm has identified...
The Issue: The firm has identified a problem with the control software for the celling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IcePearl" 2.1 CX Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Five IceSphere" Prostate Cryoablation Kit Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceRod" 1.5 CX 90¿ Cryoablation Needle¿ Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilite Freelite Mx Kappa Free Kit .M.OPT.A Recalled by The Binding Site...
The Issue: Due to customer complaints of positive bias impacting quality control. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IcePearl" 2.1 CX 90¿ Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENNOVATE MIS REMOVALKEY SHORT Recalled by Aesculap Implant Systems LLC Due...
The Issue: Fracture or breakage of the spinal fixation arm at the downtube instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE...
The Issue: The firm is recalling their products due the unapproved use of a food...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System Recalled by...
The Issue: Zimmer Biomet is conducting a medical device correction to update the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus LS - Manual Defibrillator Recalled by Remote Diagnostic Technologies...
The Issue: A software error was detected within software version 1.3.4 for the Tempus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.