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. 1,819 recalls have been distributed to North Carolina in the last 12 months.
Showing 43521–43540 of 54,363 recalls
Recalled Item: ACCU-CHEK Tender II 13/60 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 13/80 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: 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: ACCU-CHEK Tender II 17/110 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 13/110 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 17/110 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: ACCU-CHEK Tender II 13/80 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: 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: GINSENG KIANPI PIL Recalled by One and Zen Due to Undeclared Dexamethasone
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mercaptopurine Tablets Recalled by American Health Packaging Due to Failed...
The Issue: Failed USP Dissolution Test Requirements: This sub-recall is in response to...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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 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: 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: 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.