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. 2,616 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,616 in last 12 months

Showing 1706117080 of 28,688 recalls

Medical DeviceNovember 27, 2017· Cincinnati Sub-Zero Products LLC

Recalled Item: Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR...

The Issue: Due to FDA's safety communication relating to nontuberculous mycobacteria...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: ARROWg+ard BLUE PLUS Pressure Injectable Quad- Lumen CVC Kit Product...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: ARROWg+ard BLUE PLUS Pressure Injectable Two- Lumen CVC Kit Product Recalled...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue¿ Large-Bore Multi-Lumen CVC Kit Product Usage: The Arrow¿...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: AGB+ Pressure Injectable Multi- Lumen CVC Kit Product Usage: The Recalled by...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Product Usage: The Arrow¿ CVC is indicated to Recalled by...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Ethicon, Inc.

Recalled Item: DERMABOND" PRINEO" Skin Closure System Product Usage: DERMABOND PRINEO...

The Issue: Ethicon discovered that specific lots of DERMABOND"PRINEO"System may not dry...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: AGB+ Pressure Injectable Quad- Lumen CVC Kit Product Usage: The Recalled by...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: AGB+ Pressure Injectable Multi- Lumen CVC Kit Product Usage: The Recalled by...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2017· ECOLAB INC

Recalled Item: ECOLAB MICROTEK Rolled Probe Cover Recalled by ECOLAB INC Due to The...

The Issue: The incorrect IFU was shipped with the product.

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

Class III — Low RiskOngoing
Medical DeviceNovember 22, 2017· ECOLAB INC

Recalled Item: ECOLAB MICROTEK Rolled Probe Cover Recalled by ECOLAB INC Due to The...

The Issue: The incorrect IFU was shipped with the product.

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2017· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: 10 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...

The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2017· Covidien LLC

Recalled Item: Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Recalled...

The Issue: Rechargeable lithium-ion batteries with incorrect firmware that are used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2017· SANTA JOY ORNAMENT & GIFTWARE CO

Recalled Item: Santajoy Ornament & Giftware Co. Recalled by SANTA JOY ORNAMENT & GIFTWARE...

The Issue: It was discovered that the product units it imported may, at peak levels,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2017· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: 15 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...

The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2017· Elekta Limited

Recalled Item: Agility with Integrity R3.2 Recalled by Elekta Limited Due to Potential for...

The Issue: Potential for positional errors following automatic table movement (ATM).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2017· Elekta Limited

Recalled Item: Integrity R1.2 Recalled by Elekta Limited Due to Potential for positional...

The Issue: Potential for positional errors following automatic table movement (ATM).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2017· Invivo Corporation

Recalled Item: Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio...

The Issue: While in Full Disclosure playback, a user may inadvertently close the Full...

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

Class II — Potential Health HazardOngoing