Product Recalls in South Carolina
Product recalls affecting South Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to South Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 951 recalls have been distributed to South Carolina in the last 12 months.
Showing 41861–41880 of 51,854 recalls
Recalled Item: Arthrosurface HHXL (OVO) 15.6x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Myoglobin Calibrator (MYO CAL) Recalled by Siemens...
The Issue: Dimension Vista Myoglobin Calibrator (MYO CAL) may produce a positive shift...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 25&30mm 10.5x28mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydrALAZINE Hydrochloride Tablets Recalled by Par Pharmaceutical Inc. Due to...
The Issue: Presence of Foreign Substance: Par Pharmaceutical, Inc. is recalling one lot...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Autoject E1 Fixed needle device Recalled by Owen Mumford USA, Inc. Due to...
The Issue: The syringe carrier is missing components: a damper and spring.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial Double Lumen Tube Set (Right) Recalled by Teleflex, Inc. Due to...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carlens Bronchial Double Lumen Tube Set (Left) Sterile Recalled by Teleflex,...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheopart Set (Left) Recalled by Teleflex, Inc. Due to Customer complaints...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL Port A Cul tubes with Swabs Sterile Pack Recalled by Becton Dickinson &...
The Issue: The products may exhibit indications of excessive oxidation. Excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL Port A Cul tubes Recalled by Becton Dickinson & Co. Due to The products...
The Issue: The products may exhibit indications of excessive oxidation. Excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: White Bronchial Double Lumen Tube Set (Right) Sterile Recalled by Teleflex,...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial Double Lumen Tube Set (Left) Recalled by Teleflex, Inc. Due to...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheopart Set (Right) Recalled by Teleflex, Inc. Due to Customer...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial One Lumen Tube - Left Recalled by Teleflex, Inc. Due to Customer...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial Double Lumen Tube Set (Left) Recalled by Teleflex, Inc. Due to...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial One Lumen Tube - Right Recalled by Teleflex, Inc. Due to Customer...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL PT-Fibrinogen HS PLUS Recalled by Instrumentation Laboratory Co. Due...
The Issue: Some vials of HemosIL PT-Fibrinogen HS PLUS, Part No. 0008469810 (various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluorescence Imaging Procedure Kit Recalled by Intuitive Surgical, Inc. Due...
The Issue: The storage conditions for indocyanine green (ICG) are not on the individual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DrugCheck Ketamine Dip Test 31317-3P PRO-EU-SWE Recalled by Express...
The Issue: This recall has been initiated due to potential false positives results when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 Recalled by...
The Issue: Needle is not captured in the needle safety sheath in specific lots.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.