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. 2,829 recalls have been distributed to North Carolina in the last 12 months.
Showing 841–860 of 29,737 recalls
Recalled Item: AFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC. dba...
The Issue: Due to products manufactured under an inadequate quality system to include...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....
The Issue: Due to products manufactured under an inadequate quality system to include...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....
The Issue: Due to products manufactured under an inadequate quality system to include...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B105P Recalled by GE Healthcare Finland Oy Due to Potential loss of...
The Issue: Potential loss of monitoring on affected monitors when powered by certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE ONE Recalled by GE Healthcare Finland Oy Due to Potential loss of...
The Issue: Potential loss of monitoring on affected monitors when powered by certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portrait VSM Model nos. 6660000-666 Monitor Recalled by GE Healthcare...
The Issue: Potential loss of monitoring on affected monitors when powered by certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient...
The Issue: Potential loss of monitoring on affected monitors when powered by certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carescape B450 Recalled by GE Healthcare Finland Oy Due to Potential loss of...
The Issue: Potential loss of monitoring on affected monitors when powered by certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Disposable Perforator 11mm. Cranial Perforator. Recalled by Integra...
The Issue: Expansion of recall of size 14 mm Codman Disposable Perforators for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene...
The Issue: Zimmer Biomet is conducting a medical device recall for two (2) lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene...
The Issue: Zimmer Biomet is conducting a medical device recall for two (2) lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Disposable Perforator 9mm. Cranial Perforator. Recalled by Integra...
The Issue: Expansion of recall of size 14 mm Codman Disposable Perforators for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOW PROF LCKNG SCREW Recalled by Synthes (USA) Products LLC Due to Although...
The Issue: Although the etched length on the screw is correct, the length marked on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOW PROF LCKNG SCREW Recalled by Synthes (USA) Products LLC Due to Although...
The Issue: Although the etched length on the screw is correct, the length marked on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cold Form Wrap: Back Recalled by DJO, LLC Due to The IFU (Information for...
The Issue: The IFU (Information for Use) on the wrap instructs the user to heat the hot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...
The Issue: A manufacturing issue could lead to a malformed cover tube press which can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...
The Issue: A manufacturing issue could lead to a malformed cover tube press which can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC FOCUS Shears + Adaptive Tissue Technology Recalled by Stryker...
The Issue: Due to manufacturing issue, reprocessed shears, may become stuck in the "on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.