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. 1,924 recalls have been distributed to North Carolina in the last 12 months.
Showing 22221–22240 of 54,363 recalls
Recalled Item: Electrosurgical Tip Cleaner Product Usage: electrosurgical accessory...
The Issue: The sterile barrier of some devices may have been affected
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cautery Tip Cleaner Product Usage: electrosurgical accessory Recalled by...
The Issue: The sterile barrier of some devices may have been affected
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrosurgical Tip Cleaner Product Usage: electrosurgical accessory...
The Issue: The sterile barrier of some devices may have been affected
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Povidone Iodine Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major Infants' Gas Relief Drops Recalled by GCP Laboratories Inc Due to...
The Issue: Microbial Contamination of Non-Sterile Product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: In-the-Ear hearing aids Recalled by GN Hearing A/S Due to GN Hearing...
The Issue: GN Hearing received reports from our manufacturing site in US regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVENCARE G3 Blood Glucose Test Strips Recalled by Medline Industries Inc Due...
The Issue: Incomplete seal and premature expiration of individually packaged Blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Behind-the-Ear hearing aids Recalled by GN Hearing A/S Due to GN Hearing...
The Issue: GN Hearing received reports from our manufacturing site in US regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE TITANIUM NON- FILLED Recalled by Angiodynamics Inc....
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XCELA Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due to Snap...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC NON-FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemo-Drop Blood Dispenser Recalled by Biomedical Polymers, Inc. Due to The...
The Issue: The metal cannula of the device either broke and the broken piece left in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manual Diff Dropper Recalled by Biomedical Polymers, Inc. Due to The metal...
The Issue: The metal cannula of the device either broke and the broken piece left in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eversense CGM SENSOR (FG-4200-00-301)-Continuous Glucose Monitor Recalled by...
The Issue: Eversense Sensors have prematurely stopped functioning due to inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the Recalled by...
The Issue: Potential ability to leak once used for compounding.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Hydroclhoride Jelly USP Recalled by Akorn, Inc. Due to cGMP...
The Issue: cGMP Deviations: firm reported finding metal particulate matter in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SE Grocers **BAKERY** 18 CT Variety Pack Cookies Recalled by SOUTHEASTERN...
The Issue: 18 count Variety Pack cookies made in-store bakeries included Peanut Butter...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SE Grocers **BAKERY** 18 CT Peanut Butter Cookies Recalled by SOUTHEASTERN...
The Issue: 18 count Peanut Butter cookies made in-store bakeries failed to declare...
Recommended Action: Do not consume. Return to store for a refund or discard.