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. 2,467 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,467 in last 12 months

Showing 1434114360 of 27,558 recalls

Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: MR RT Recalled by Philips Medical Systems Nederlands Due to There is a...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Intera IT Recalled by Philips Medical Systems Nederlands Due to There is a...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Ingenia 1.5T CX Recalled by Philips Medical Systems Nederlands Due to There...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: MR-OR 1.5T Recalled by Philips Medical Systems Nederlands Due to There is a...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Multiva 1.5T Recalled by Philips Medical Systems Nederlands Due to There is...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Multiva 1.5T 16 R5 Recalled by Philips Medical Systems Nederlands Due to...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Ingenia Ambition S Recalled by Philips Medical Systems Nederlands Due to...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Intera 1.0T Omni/Stellar Recalled by Philips Medical Systems Nederlands Due...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Achieva 1.5T High Performance Recalled by Philips Medical Systems Nederlands...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Intera 3.0T Master/Quasar Dual Recalled by Philips Medical Systems...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Achieva 3.0T Recalled by Philips Medical Systems Nederlands Due to There is...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Prodiva CS Recalled by Philips Medical Systems Nederlands Due to There is a...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Ingenia 1.5T Recalled by Philips Medical Systems Nederlands Due to There is...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· TERRIFIC CARE LLC

Recalled Item: CoaguChek XS PT Test Recalled by TERRIFIC CARE LLC Due to Potential for...

The Issue: Potential for abnormally high INR test results with the CoaguChek XS PT Test...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Centricity Universal Viewer Breast Imaging Centricity...

The Issue: When switching back & forth between multiple UV instances in the Windows...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· Merge Healthcare, Inc.

Recalled Item: The WinStation Retinal Imager Recalled by Merge Healthcare, Inc. Due to...

The Issue: Certain configurations of Merge Eye Station hardware may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Cincinnati Sub-Zero...

The Issue: Evidence supports that when customers performed a fuse replacement as part...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF PET/CT (non-RoHS) Recalled by Philips Medical Systems...

The Issue: A software update is being issued to correct multiple issues identified in...

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

Class II — Potential Health HazardOngoing