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. 1,042 recalls have been distributed to North Carolina in the last 12 months.
Showing 21201–21220 of 54,363 recalls
Recalled Item: TRIMIX -A (UA) 30MG/1MG/5 MCG/ML INJ in 1 mL vial Recalled by Assurance...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BAC 200MCG/BUP22MG/CLON210MCG/HYDROM 15MG/SUF800MCG/ML ML INJ in 20 mL...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUP 30MG/ FENT 400MCG/ML INJ in 20 mL syringe Assurance Recalled by...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MORPHINE 5MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUP 5MG/MORP 10MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENOL 2.5% STERILE SOLUTION in 50 mL syringe Assurance Infusion Recalled by...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MORPHINE 30MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUP 2.5MG/ CLONI 5MCG/ FENT 200MCG/ SUF 50MCG/ML (40) INJ Recalled by...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUP 17MG/MORP 22MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUP 23MG/HYDROM 25MG/SUF 100MCG/ML INJ in 20 mL syringe Assurance Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or...
The Issue: Monitor/Defibrillator may not deliver a shock after the "Shock" button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits Recalled by Physio-Control,...
The Issue: Monitor/Defibrillator may not deliver a shock after the "Shock" button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The potential exists for system movement to be permanently blocked by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamotrigine Tablets Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...
The Issue: Cross Contamination; Lamotrigine Tablets 100 mg USP was contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CombiDiagnost GCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...
The Issue: When using the Table Up/Down button, the system may experience Error 80,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION PS High Flex XLPE size 5-6 9mm Articular Insert Recalled by Smith &...
The Issue: LEGION PS High Flex XLPE Articular Insert was packaged with an incorrect part
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...
The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Daytona Plus (with ISE/without ISE) Recalled by Randox Laboratories,...
The Issue: Software version UI2550642107 for the RX Daytona + instrument released to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost PCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...
The Issue: When using the Table Up/Down button, the system may experience Error 80,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...
The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.