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 2132121340 of 27,558 recalls

Medical DeviceJune 29, 2015· Becton Dickinson & Co.

Recalled Item: Enterococcus Screen Agar QUAD Plate Recalled by Becton Dickinson & Co. Due...

The Issue: The affected expired lots of product may have exhibited breakthrough growth...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam Gamma Camera Recalled by Siemens Medical Solutions USA, Inc. Due to...

The Issue: Potential failure mode related to the radial brake, where the detector was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Alere Scarborough, Inc. dba Binax, Inc.

Recalled Item: Alere i flu Recalled by Alere Scarborough, Inc. dba Binax, Inc. Due to Risk...

The Issue: Risk of false negative results due to microbial growth in the Sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BEA Broth with Vancomycin container type: 13x100mm tube...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BEA Agar with Vancomycin container type: 15x100mm...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics MacConkey Agar with CiPRP Recalled by Hardy Diagnostics...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics MDR Acinetobacter container type: 15x100mm monoplate...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BHI with CIPRO Recalled by Hardy Diagnostics Due to Hardy...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics VRE Broth Recalled by Hardy Diagnostics Due to Hardy...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BEA Agar with VGA container type: 15x100mm monoplate...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON S2000 and ACUSON S3000 ultrasound systems with the Virtual Recalled...

The Issue: Potential measurement error on ACUSON S Family ultrasound system. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON S 1000 Recalled by Siemens Medical Solutions USA, Inc. Due to...

The Issue: Potential measurement error on ACUSON S Family ultrasound system when using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· Zimmer Surgical Inc

Recalled Item: 30inch Dual Port/Single Bladder Disposable Tourniquet Cuff with PLC Recalled...

The Issue: The inside of the folded Instructions For Use (IFU) pamphlet was missing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· Zimmer Surgical Inc

Recalled Item: 18inch Dual Port/Single Bladder Disposable Tourniquet Cuff Recalled by...

The Issue: The inside of the folded Instructions For Use (IFU) pamphlet was missing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· EKOS Corporation

Recalled Item: The EKOS EkoSonic Control Unit is intended exclusively for use Recalled by...

The Issue: The Connector Interface Cable (CIC) was not recognized by the EkoSonic PT-3B...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Prism Medical P-600 Portable Ceiling Lift Recalled by ErgoSafe Products, LLC...

The Issue: There is a potential the sling loops may not stay attached to the carry bar...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Prism Medical P-440 Portable Ceiling Lift Recalled by ErgoSafe Products, LLC...

The Issue: There is a potential the sling loops may not stay attached to the carry bar...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes TI Matrix Pre-Bent Maxillary Plate / 2mm ADVMNT/0.8mm THK/L Recalled...

The Issue: The affected part and lot numbers of the TI Matrix Pre-Bent Maxillary Plates...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2015· O-Two Medical Technologies, Inc.

Recalled Item: O-Two Adult Ventilation Timer Recalled by O-Two Medical Technologies, Inc....

The Issue: Malfunction of an O-Two Adult Ventilation Timer, where the flash rate of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Volcano Corporation

Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems with software versions...

The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...

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

Class II — Potential Health HazardOngoing