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. 2,516 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,516 in last 12 months

Showing 78417860 of 27,558 recalls

Medical DeviceJune 17, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin.net model MN5000 Software Recalled by St. Jude Medical, Cardiac...

The Issue: The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2022· Luminex Corporation

Recalled Item: VERIGENE Enteric Pathogens Nucleic Acid Test Recalled by Luminex Corporation...

The Issue: There is a potential for false negative results using VERIGENE CDF Stool...

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 ob/gyn 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 Angiography packs/trays Recalled by American Contract Systems, Inc....

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: 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