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. 1,932 recalls have been distributed to North Carolina in the last 12 months.
Showing 21021–21040 of 54,363 recalls
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medonic M-Series Hematology Analyzer M16S BD ABR US Product code: 1400075...
The Issue: A mix-up of autosampler tube positions with a possibility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Savannah Classics Classic Bread Stuffing packaged in 4.5lb trays Recalled by...
The Issue: Eggs used in the manufacture of the products may be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Morrison's cornbread dressing packaged in 7lb trays Recalled by Savannah...
The Issue: Eggs used in the manufacture of the products may be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Morrison's cornbread dressing packaged in 4lb tray Recalled by Savannah Food...
The Issue: Eggs used in the manufacture of the products may be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Piccadilly Cornbread Dressing in 2# trays Recalled by Savannah Food Company,...
The Issue: Eggs used in the manufacture of the products may be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Savannah Classics Classic Cornbread Dressing packaged in 7lb trays Recalled...
The Issue: Eggs used in the manufacture of the products may be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Savannah Classics Special Cornbread Dressing packaged in 7lb trays Recalled...
The Issue: Eggs used in the manufacture of the products may be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Integris Allura 9 Recalled by Philips North America, LLC Due to A capacitor...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardio Vascular-Allura Centron Recalled by Philips North America, LLC Due to...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroDiagnost Eleva Recalled by Philips North America, LLC Due to A capacitor...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniDiagnost Eleva System codes 708028 708027 Recalled by Philips North...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integris Allura 15 & 12 Recalled by Philips North America, LLC Due to A...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva Recalled by Philips North America, LLC Due to A...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Poly G Integris H5000 Recalled by Philips North America, LLC Due to A...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.