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. 2,124 recalls have been distributed to North Carolina in the last 12 months.
Showing 2821–2840 of 54,363 recalls
Recalled Item: PHENYLephrine HCl in 0.9% Sodium Chloride Recalled by Denver Solutions, LLC...
The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketamine HCl 50mg per 5mL (10 mg per mL) Recalled by Denver Solutions, LLC...
The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glycopyrrolate Recalled by Denver Solutions, LLC DBA Leiters Health Due to...
The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: dexmedeTOMIDine HCl PF Recalled by Denver Solutions, LLC DBA Leiters Health...
The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bimatoprost powder Recalled by Medisca Inc. Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rocuronium Bromide 50 mg per 5mL (10mg per mL) Recalled by Denver Solutions,...
The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Straight Inflow/Outflow Patient Line Kit. Model Number: 902-00037. Sterile...
The Issue: Potential crack in the female connector located on the Heat Exchanger in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Inflow/Bifurcated Outflow Line Kit. Model Number: 902-00038....
The Issue: Potential crack in the female connector located on the Heat Exchanger in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trader Joe's Hot Honey Mustard Dressing (SKU #80152) Recalled by Reser's...
The Issue: Undeclared peanuts, soy, sesame, and wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:...
The Issue: Potential for early life x-ray tube failure for mobile x-ray system due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guide Wire with Ruler Tube 3x800 mm DIA Recalled by Stryker GmbH Due to The...
The Issue: The metal ring at the end of the Guide Wire with Ruler Tube may detach from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:...
The Issue: Potential for early life x-ray tube failure for mobile x-ray system due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guide Wire with Ruler Tube 3x1000 mm DIA Recalled by Stryker GmbH Due to The...
The Issue: The metal ring at the end of the Guide Wire with Ruler Tube may detach from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B Braun Interventional ELITE HV Hemostasis Valve Introducer System by Galt...
The Issue: Due to a potential open seal in the sterile barrier packaging .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraocular lens. enVista Monofocal IOL Recalled by Bausch & Lomb Surgical,...
The Issue: In response to an increased number of reports of toxic anterior segment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GALT Centeze Catheter DRC-002-06 The Centeze is intended Recalled by Galt...
The Issue: Due to a potential open seal in the sterile barrier packaging .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraocular Lens. enVista Envy IOL Recalled by Bausch & Lomb Surgical, Inc....
The Issue: In response to an increased number of reports of toxic anterior segment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introducer Kit- Coaxial Dilator Recalled by Galt Medical Corporation Due to...
The Issue: Due to a potential open seal in the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount Recalled by IHB OPERATIONS...
The Issue: The mounting hardware that is supplied with the 4FXS-60 monitor bracket does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introducer Kit- Tearaway MicroSlide Recalled by Galt Medical Corporation Due...
The Issue: Due to a potential open seal in the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.