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. 2,789 recalls have been distributed to North Carolina in the last 12 months.
Showing 8221–8240 of 29,737 recalls
Recalled Item: EIT CIF cage Recalled by DePuy Spine, Inc. Due to Label on the Outer Carton...
The Issue: Label on the Outer Carton does not match the labels on the Outer Blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensica Urine Output System Recalled by C.R. Bard Inc Due to Complaints...
The Issue: Complaints relating to urine output measurement accuracy.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MODULAR CATHCART FRACTURE HEAD HIP BALL Recalled by DePuy Orthopaedics, Inc....
The Issue: The Cathcart Ball has an inherent +5mm offset which is not currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension LTNI -In vitro diagnostic test intended to quantitively measure...
The Issue: Positive bias with Lithium Heparin plasma samples from individuals that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension CTNI-In vitro diagnostic test intended to quantitively measure...
The Issue: Positive bias with Lithium Heparin plasma samples from individuals that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 Flex Analyzer Model Numbers 393-800 and 393-801 Recalled by...
The Issue: There is a potential for sporadic incidents of positive and negative biases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: #1 MAC F/O LARYNGOSCOPE Recalled by Baxter Healthcare Corporation Due to...
The Issue: Packaging error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drager SafeStar 55 Recalled by Draeger Medical, Inc. Due to Possible...
The Issue: Possible occlusion of filters due to manufacturing error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one...
The Issue: The outer package is mislabeled and the package contains a different IOL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA Autosuture Circular Stapler with DST Series Technology Recalled by...
The Issue: The affected staplers have the potential for the staple guide to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...
The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...
The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Pill Splitters Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Product lid (which houses a blade) is coming unhinged from the base, thus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE Central Station (CSCS) V2 Recalled by GE Healthcare, LLC Due to...
The Issue: The CARESAPE Central Station (CSCS) V2 can shut down due to a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394600 (OUS)...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS) Recalled by...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nexiva with Single BD Connecta Stopcock Version (20 Ga Blue) Recalled by...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.