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. 2,763 recalls have been distributed to North Carolina in the last 12 months.
Showing 10661–10680 of 29,737 recalls
Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...
The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Humidification Flask Recalled by Cook Medical Llc Due to A small...
The Issue: A small percentage of the Disposable Humidification Flasks may have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips EPIQ Diagnostic Ultrasound System Recalled by Philips Ultrasound Inc...
The Issue: The manufacturer discovered an issue associated with the EPIQ Image Boost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STI(TM) Recalled by Microbiologics Inc Due to The expiration date on...
The Issue: The expiration date on the label of one component (negative control 0243U)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUITY Universal Cutter Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific (BSC) is retrieving five Model 7060 ACUITY cutters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORTEX Bivona Cuffless Neonatal/Pediatric FlexTend Tracheostomy Tube...
The Issue: A specific model and lot number of Bivona Cuffless FlexTend Tracheostomy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT Chemistry Products ALB-TP Slides (ALB is not affected) Recalled by...
The Issue: Eltrombopag Interference for VITROS Chemistry Products TP Slides and VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products TP Slides- IVD measure total protein (TP) Recalled...
The Issue: Eltrombopag Interference for VITROS Chemistry Products TP Slides and VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WAHL 4212 HEATED MASSAGER Recalled by Wahl Clipper Corp Due to The...
The Issue: The connection between the massager and heat element can overheat causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7MAX KIT Penumbra JET 7 Reperfusion Catheter+ MAX Recalled by...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle Cups Recalled by DePuy Orthopaedics, Inc. Due to Certain Pinnacle...
The Issue: Certain Pinnacle Cup devices may potentially exhibit an oversized "minor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7 Reperfusion Catheter The Penumbra JET Recalled by Penumbra...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENOVO Venous Stent System 10F Product Description(REF)/dimension:...
The Issue: Reports of the proximal end of the stent not immediately expanding upon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuroreader Medical Image Processing Software - Product Usage: intended to...
The Issue: The Neuroreader has been distributed with a normative database that is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bactiseal Endoscopic Ventricular Catheter: EVC- Catheter is designed for use...
The Issue: Mislabeled product-Bactiseal Ventricular Catheter with Bactiseal Shunt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA dsDNA Well - Product Usage: intended for the In-Vitro Recalled by...
The Issue: Decreased values for EliA ANA Positive Control when using the EliA dsDNA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bactiseal Ventricular Catheter with Bactiseal Shunt System - Product Usage:...
The Issue: Mislabeled product-Bactiseal Ventricular Catheter with Bactiseal Shunt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENOVO Venous Stent System 8F Product Description(REF)/dimension: VENEL10040...
The Issue: Reports of the proximal end of the stent not immediately expanding upon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.