Product Recalls in South Dakota

Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,491 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,491 in last 12 months

Showing 1156111580 of 47,632 recalls

Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Breast Abdominoplasty Pack Recalled by American Contract Systems, Inc. Due...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various C-section packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various convenience packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various convenience packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: D&C pack Recalled by American Contract Systems, Inc. Due to Product was...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Port Insertion Packs Recalled by American Contract Systems, Inc. Due...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various eye packs Recalled by American Contract Systems, Inc. Due to Product...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various neurology packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Pacemaker Packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various ENT Packs Recalled by American Contract Systems, Inc. Due to Product...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Angiography/Cath Lab packs/trays Recalled by American Contract...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Cysto Packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various hysterectomy Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Laparoscopy Packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various PICC Line Recalled by American Contract Systems, Inc. Due to Product...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...

The Issue: Internal ethernet cable may be misaligned, the cable jacket (insulation)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· NordicNeuroLab AS

Recalled Item: nordicBrainEX Recalled by NordicNeuroLab AS Due to When exporting merged...

The Issue: When exporting merged results from the BOLD, DSC, and DCE modules of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...

The Issue: Internal ethernet cable may be misaligned, the cable jacket (insulation)...

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

Class II — Potential Health HazardOngoing
DrugJune 15, 2022· Vi-Jon, LLC

Recalled Item: 70% ISOPROPYL ALCOHOL First aid antiseptic Recalled by Vi-Jon, LLC Due to...

The Issue: Defective Container: Product may leak when squeezed or when not in an...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJune 15, 2022· Premier Research Labs LLC

Recalled Item: AloePro Dietary Supplement Made With Organic ALOE VERA LIQUID 16 Recalled by...

The Issue: Product spoiling over time; spoilage visible beneath lid/closure upon opening.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund