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. 2,705 recalls have been distributed to South Carolina in the last 12 months.
Showing 8741–8760 of 28,688 recalls
Recalled Item: GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...
The Issue: Reports have been received of tip damage during use of the devices which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...
The Issue: Reports have been received of tip damage during use of the devices which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...
The Issue: There is a potential for abnormal (non-sigmoidal) amplification curves.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...
The Issue: There is a software issue associated with the ability to properly complete a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing...
The Issue: lmagePilot versions 1.92 and 1.93 paired with an AeroDR or Momentum Panel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw Recalled by Wright...
The Issue: Incorrect product is contained in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPELA FHD PTZ TILE KITS with Axis cameras used in Recalled by Natus...
The Issue: Tile kits that allow one to install and situate a video camera within a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Michels Transport Medium Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Product stored incorrectly in temperature controlled setting instead of .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARDY DIAGNOSTICS CatScreen Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Product stored incorrectly in temperature controlled setting instead of .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Celltrion DiaTrust COVID-19 Ag Rapid Test Recalled by CELLTRION USA INC Due...
The Issue: The European version of the DiaTrust COVID-19 Ag Rapid Test is not approved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Rotaclone Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Product stored incorrectly in temperature controlled setting instead of .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH ¿2-Microglobulin (B2M) -M) Assay for in vitro diagnostic...
The Issue: ¿2 Microglobulin (B2M) Reagent Lot 211446 Bias with Quality Control and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemashield Gold Knitted Bifurcated Recalled by Maquet Cardiovascular, LLC...
The Issue: There is a probable mislabeling of product. A Hemashield Platinum Woven...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 Article Number: 138.107...
The Issue: Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.