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. 1,897 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,897 in last 12 months

Showing 72017220 of 47,632 recalls

Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· GE Hangwei Medical Systems, Co. LTD

Recalled Item: The System is designed as a modular system with components Recalled by GE...

The Issue: GE HealthCare has become aware of the potential that incorrect torque has...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Axillary Insertion Introducer -Introducer(s) are intended for...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Introducer Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Oscor Intro Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
DrugNovember 7, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Indomethacin 25mg Capsules Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 7, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Naproxen Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2023· Bayer Healthcare Pharmaceuticals Inc.

Recalled Item: VITRAKVI (larotractenib) oral solution Recalled by Bayer Healthcare...

The Issue: Microbial Contamination of Non-Sterile Products: microbial contamination...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 6, 2023· Taro Pharmaceuticals Inc.

Recalled Item: Hydrocortisone 1% and Acetic Acid 2% Otic Solution USP Recalled by Taro...

The Issue: Failed Impurities/Degradation Specifications:Out-of-Specification result for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 6, 2023· Nurse Assist, LLC

Recalled Item: Sterile Water/Saline: Product Name/Product Code: CUP STERILE WATER¿ FOIL LID...

The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2023· Nurse Assist, LLC

Recalled Item: 0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL:...

The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2023· Merit Medical Systems, Inc.

Recalled Item: Fountain Recalled by Merit Medical Systems, Inc. Due to The sterility of...

The Issue: The sterility of microcatheter and infusion system devices cannot be guaranteed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2023· Nurse Assist, LLC

Recalled Item: Sterile Water: Product Name/Product Code: USP STERILE WATER SYRINGE/1030A...

The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2023· Physio-Control, Inc.

Recalled Item: AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator Recalled...

The Issue: AC Power Adapter (ACPA) may not charge the monitor/defibrillator batteries...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2023· Nurse Assist, LLC

Recalled Item: Sterile Water/Saline: Brand Name: Product Name/Product Code: CARDINAL: 100ML...

The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2023· Merit Medical Systems, Inc.

Recalled Item: Merit Maestro Microcatheter Recalled by Merit Medical Systems, Inc. Due to...

The Issue: The sterility of microcatheter and infusion system devices cannot be guaranteed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2023· Sarnova HC, Llc

Recalled Item: Curaplex Field Cric Kit with ET Tube Recalled by Sarnova HC, Llc Due to It...

The Issue: It was determined that the Endotracheal Tube Holder included in certain kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2023· Merit Medical Systems, Inc.

Recalled Item: Merit Pursue Microcatheter Recalled by Merit Medical Systems, Inc. Due to...

The Issue: The sterility of microcatheter and infusion system devices cannot be guaranteed.

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

Class II — Potential Health HazardOngoing