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. 2,386 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,386 in last 12 months

Showing 2084120860 of 27,558 recalls

Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT SELF REGIONAL HEALTHCARE PV LEG PACK Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT RENOWN REGIONAL MEDICAL CENTER Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA MASTER DVD V4.0 CLI Product Usage: MYLA is a Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA MASTER DVD V4.1 CLI Product Usage: MYLA is a Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA CLINIC PATCH 3.3.0 CD Product Usage: MYLA is a Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA CLI V3.X TO V4.1 DL380 SERVER Product Usage: MYLA Recalled by...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA CLI V3.X TO V4.1 ML350 SERVER Product Usage: MYLA Recalled by...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA MASTER DVD 3.2 CLI DL380 Product Usage: MYLA is Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA CLINIC PATCH 3.2.0 CD Product Usage: MYLA is a Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD10 Recalled by Philips Electronics North America Corporation...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: INTEGRIS V3000 Recalled by Philips Electronics North America Corporation Due...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD10/10 Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: INTEGRIS CV Recalled by Philips Electronics North America Corporation Due to...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20/10 Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20/20 OR Table Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 15-12 (biplane) Recalled by Philips Electronics North...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD10 OR Table Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing