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. 1,913 recalls have been distributed to North Carolina in the last 12 months.
Showing 24161–24180 of 29,737 recalls
Recalled Item: ACCU-CHEK Tender II 17/80 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender II 17/60 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender I 17/80 10 pieces Product Usage: Intended for Recalled by...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lithium Polymer Fiber Optic Module Batteries used in the Intera Recalled by...
The Issue: VCG battery ignited in a VCG unit when recharging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECG Out Cable Recalled by Philips Electronics North America Corporation Due...
The Issue: When a Philips monitor/defibrillator is receiving an ECG signal from an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models:M3535A Recalled by...
The Issue: MRx Defib can be susceptible to one or both issues: 1. The C02 Inlet Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Models: M3535A and M3536A...
The Issue: 1. Device will perform the weekly automated tests hourly, which could cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue TcG10 Recalled by Philips Medical Systems, Inc. Due to...
The Issue: Philips has discovered that the Instructions for Use (IFU) for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...
The Issue: Device may malfunction, which could cause therapy to be delayed, disabled,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CelluTome Epidermal Harvesting System Harvester (5.0 CM) STERILE EO Rx...
The Issue: KCI has received reports that, in a small number of cases, the CelluTome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lite DM (Lite Data Manager) Software Version(s): Versions 2.0.0.19 and...
The Issue: HORIBA Medical is informing all HORIBA Medical Lite DM customers using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.