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. 1,716 recalls have been distributed to South Carolina in the last 12 months.
Showing 48801–48820 of 51,854 recalls
Recalled Item: Voltaren 1% Gel Recalled by Physicians Total Care, Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date; This recall is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brunswick and Bumble Bee Brand 5oz Chunk Light Tuna in Water. Recalled by...
The Issue: Bumble Bee Foods, LLC, has issued a voluntary recall on specific codes of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bumble Bee Brand 5oz Chunk Light Tuna in Vegetable Oil Recalled by Bumble...
The Issue: Bumble Bee Foods, LLC, has issued a voluntary recall on specific codes of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jasmine Brand Garlic Flavored Crackers (Krupuk Bawang) Recalled by Jans...
The Issue: Wira Corp. is recalling Jasmine Garlic Flavored Crackers because of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bumble Bee Brand 5oz Chunk White Albacore in Water Recalled by Bumble Bee...
The Issue: Bumble Bee Foods, LLC, has issued a voluntary recall on specific codes of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roche Molecular Systems cobas x 480 System 50 mL reagent reservoir Recalled...
The Issue: Certain lots of Reagent reservoirs, may not have a separation in the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diacap(R) Ultra Dialysis Fluid Filter Recalled by B. Braun Medical, Inc. Due...
The Issue: There is the potential of the residual moisture of the Diacap Ultra membrane...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...
The Issue: American Medical Systems, Inc. is initiating a recall on two components of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific/Cameron Health SQ-RX Model 1010 subcutaneous pulse...
The Issue: An internal protective fuse can be unintentionally activated while the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...
The Issue: American Medical Systems, Inc. is initiating a recall on two components of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mammomat Inspiration - full-field digital mammography Product Usage:...
The Issue: Firm became aware of an unintended behavior when using the Mammomat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Venous blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial and Venous Recalled...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial and Venous Recalled...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet EEG Wireless Amplifier 32/64 Channel. Catalog/Part Numbers :...
The Issue: Natus Neurology Incorporated is recalling the Nicolet EEG Wireless Amplifier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular Solutions Recalled by Vascular Solutions, Inc. Due to Risk that air...
The Issue: Risk that air may be introduced into the device which may lead to an air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirtex SIR-yttrium 90 microspheres (Radionuclide) Recalled by Sirtex Medical...
The Issue: Incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Prostiva RF Therapy Generator. The Prostiva RF system is Recalled...
The Issue: Medtronic has found through device testing that if the optional footswitch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.