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. 2,349 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,349 in last 12 months

Showing 2616126180 of 47,632 recalls

Medical DeviceDecember 8, 2017· Zimmer Biomet, Inc.

Recalled Item: Humeral Stem 55mm(Size 13) Product Usage: Intended for primary and Recalled...

The Issue: Zimmer Biomet is conducting a medical device recall for two lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Abbott Laboratories, Inc

Recalled Item: ARCHITECT c4000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...

The Issue: There is a potential to generate falsely depressed patient results in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Abbott Laboratories, Inc

Recalled Item: ARCHITECT c8000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...

The Issue: There is a potential to generate falsely depressed patient results in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Zimmer Biomet, Inc.

Recalled Item: Humeral Stem 83mm(Size 17) Product Usage: Intended for primary and Recalled...

The Issue: Zimmer Biomet is conducting a medical device recall for two lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Remel Inc

Recalled Item: Remel Shigella sonnei Phase 1 & 2 Agglutinating Serum Recalled by Remel Inc...

The Issue: The serum may fail to agglutinate within the specified minimum reaction time.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Datex-Ohmeda, Inc.

Recalled Item: CARESCAPE R860 ventilators with software version 10SP05 Product Usage: The...

The Issue: Potential for the display processor to experience an unexpected failure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: PROPONENT EL DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE MRI EL DR Pacemaker Recalled by Boston Scientific Corporation Due...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: VISIONIST CRT-P Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: PROPONENT SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: PROPONENT DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: VALITUDE CRT-P Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE MRI DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE MRI SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ALTRUA 2 SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO MRI SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ALTRUA 2 EL DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO MRI EL DR Pacemaker Recalled by Boston Scientific Corporation Due...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing