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. 2,672 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,672 in last 12 months

Showing 1156111580 of 28,688 recalls

Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris System PC Unit Model 8000 Recalled by CareFusion 303, Inc. Due to...

The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris Auto ID Module Model 8600 Recalled by CareFusion 303, Inc. Due to...

The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 29, 2020· Smith & Nephew, Inc.

Recalled Item: PERI-LOC TARGETER 4.5MM DISTAL FEMUR Recalled by Smith & Nephew, Inc. Due to...

The Issue: The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2020· Precision Valve & Automation,Inc

Recalled Item: PVA Recalled by Precision Valve & Automation,Inc Due to While operating the...

The Issue: While operating the machine in "Run" mode an unexcepted event may occur...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2020· RANDOX LABORATORIES, LTD.

Recalled Item: Randox Lipase Assay: Lipase Colorimetric R2 Substrate - Product Usage:...

The Issue: Randox have confirmed imprecision of quality control and patient samples...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2020· Boss Instruments, Ltd.

Recalled Item: BOSS DeBakey "Gator-Grip" Needle Holder 2 mm tip Recalled by Boss...

The Issue: The tungsten carbide plate, which is intended to hold the sewing needle...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2020· RANDOX LABORATORIES, LTD.

Recalled Item: Randox Lipase Assay: Lipase Colorimetric R1 Buffer - Product Usage: Recalled...

The Issue: Randox have confirmed imprecision of quality control and patient samples...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2020· RANDOX LABORATORIES, LTD.

Recalled Item: Randox Lipase Assay: Lipase Colorimetric Reagent - Product Usage: A Recalled...

The Issue: Randox have confirmed imprecision of quality control and patient samples...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2020· Steris Corporation

Recalled Item: InnoWave Sonic Irrigator Recalled by Steris Corporation Due to A recent FDA...

The Issue: A recent FDA inspection at the firm identified that the foil test performed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2020· Philips North America, LLC

Recalled Item: IntelliVue G7m Anesthesia Gas Module Recalled by Philips North America, LLC...

The Issue: The device may experience an interruption of gas measurement due to a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2020· DNA Genotek Inc.

Recalled Item: PrepIT Q2A Kit Recalled by DNA Genotek Inc. Due to Reagents were shipped to...

The Issue: Reagents were shipped to customers after the Use by data indicated on its...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJune 24, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite with software versions syngo.via VB30 or VB40...

The Issue: If the user modifies for any reason (e.g. reduction of artifacts) the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2020· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew T-F1X0 RCG Drill Pac Recalled by Smith & Nephew, Inc. Due to...

The Issue: The T-Fix sterile package contains only one sleeve instead of two, The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Chengdu Ai Qin E-commerce Co., Ltd

Recalled Item: TTDEYE (brand) Devil Red Recalled by Chengdu Ai Qin E-commerce Co., Ltd Due...

The Issue: Colored contact lenses were distributed without FDA clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Chengdu Ai Qin E-commerce Co., Ltd

Recalled Item: TTDEYE (brand) Black Starshine Recalled by Chengdu Ai Qin E-commerce Co.,...

The Issue: Colored contact lenses were distributed without FDA clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Chengdu Ai Qin E-commerce Co., Ltd

Recalled Item: TTDEYE (brand) Radial Brown Recalled by Chengdu Ai Qin E-commerce Co., Ltd...

The Issue: Colored contact lenses were distributed without FDA clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Sutter Medizintechnik GmbH

Recalled Item: Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re...

The Issue: The label on the cardbox and the blister show the correct symbols for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Chengdu Ai Qin E-commerce Co., Ltd

Recalled Item: TTDEYE (brand) Flower Brown Recalled by Chengdu Ai Qin E-commerce Co., Ltd...

The Issue: Colored contact lenses were distributed without FDA clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Chengdu Ai Qin E-commerce Co., Ltd

Recalled Item: TTDEYE (brand) Radial Pink Recalled by Chengdu Ai Qin E-commerce Co., Ltd...

The Issue: Colored contact lenses were distributed without FDA clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Chengdu Ai Qin E-commerce Co., Ltd

Recalled Item: TTDEYE (brand) Flower Grey Recalled by Chengdu Ai Qin E-commerce Co., Ltd...

The Issue: Colored contact lenses were distributed without FDA clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing