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. 1,896 recalls have been distributed to North Carolina in the last 12 months.
Showing 28161–28180 of 54,363 recalls
Recalled Item: ProCair Mattress: (a) PROCAIR PLUS 42X80 Recalled by Joerns Healthcare Due...
The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...
The Issue: The devices may have been assembled with an internal component that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics North...
The Issue: The MRx monitor/defibrillators could fail to charge because the therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Clip Gun Magazines are packaged in individually sealed pouches...
The Issue: The packaging sterile barrier does not comply with the applicable packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...
The Issue: The devices may have been assembled with an internal component that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tearaway Introducers Recalled by Galt Medical Corporation Due to The...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagNA Pure 24 System Recalled by Roche Molecular Systems, Inc. Due to...
The Issue: Cross-contamination of samples has been reported when running the existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew ANTHOLOGY POROUS HIGH OFFSET STEM Recalled by Smith & Nephew,...
The Issue: Three lots of Anthology HO Porous size 7 stems were manufactured with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centeze Centesis Catheter Recalled by Galt Medical Corporation Due to The...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) TVS LPA Recalled by Galt Medical Corporation Due to The products listed...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part #: SAM XT-C Recalled by The Seaberg Company Inc Due to Based on...
The Issue: Based on internal testing, results indicated a possible failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis Recalled by...
The Issue: The bottles are mislabeled with an incorrect part number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ELITE HV Recalled by Galt Medical Corporation Due to The products listed...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Drainer Centesis Catheter Recalled by Galt Medical Corporation Due to The...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TVS LPA Recalled by Galt Medical Corporation Due to The products listed...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Vascular Dilator Recalled by Galt Medical Corporation Due to The products...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part #: SAM XT-M Recalled by The Seaberg Company Inc Due to Based on...
The Issue: Based on internal testing, results indicated a possible failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part #: SAM XT-C Recalled by The Seaberg Company Inc Due to Based on...
The Issue: Based on internal testing, results indicated a possible failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartware Medtronic HVAD System for cardiac use. Including the following...
The Issue: Possible transient electrical connection interruption between an HVAD System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elite HV Introducer Recalled by Galt Medical Corporation Due to The products...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.