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 1428114300 of 27,558 recalls

Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Bander Ureteral Diversion Open-End Stent Set Recalled by Cook Inc. Due to...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Kwart Retro-Inject Ureteral Stent Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Wilson-Cook Medical Inc.

Recalled Item: Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical...

The Issue: Complaints of the snare loop not completely retracting and/or misshaping of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2019· Abbott Laboratories, Inc

Recalled Item: ARCHITECT MAGNESIUM Recalled by Abbott Laboratories, Inc Due to Abbott...

The Issue: Abbott internal testing has identified that the Magnesium urine application...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2019· Leica Microsystems, Inc.

Recalled Item: Leica M220 F12 surgical microscope The Leica M220 F12 surgical Recalled by...

The Issue: The M220 optics may unintentionally drop into the surgical field, risking...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2018· Cardinal Health 200, LLC

Recalled Item: Curity All Purpose Sponges Recalled by Cardinal Health 200, LLC Due to...

The Issue: Curity All Purpose Sponges were not sterilized and distributed

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2018· Luminex Corporation

Recalled Item: Vergene Amplification Tray - 700uL Recalled by Luminex Corporation Due to On...

The Issue: On lot of VERIGENE(R) BC-GP Utility Kits (20-011-018) were labeled with the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 26, 2018· Varian Medical Systems, Inc.

Recalled Item: Eclipse(TM) Treatment Planning System with Proton Convolution Superposition...

The Issue: There is an anomaly with the Eclipse(TM) Treatment Planning System [TPS]...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2018· Steris Corporation

Recalled Item: ATLAS Loading Car Recalled by Steris Corporation Due to The ATLAS loading...

The Issue: The ATLAS loading car may not remain fully engaged with the latch on the...

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 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: Intera Achieva 1.5T Nova 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: Intera 1.5T 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: Ingenia 1.5T S 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: MARLIN 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: MR-OR 3.0T 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: Achieva 7.0T 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: Intera 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: NZM101 Ingenia 1.5T Linac 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 3.0T X 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: Achieva 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