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. 2,360 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,360 in last 12 months

Showing 2550125520 of 27,558 recalls

Medical DeviceApril 22, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: HB1C Flex(R) Reagent Cartridge (DF105A Recalled by Siemens Healthcare...

The Issue: Positive bias on the lots listed compared to alternate methods and a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2013· Brainlab AG

Recalled Item: Brainlab Cranial Navigation System: An Image Guided Surgery System /...

The Issue: Software Error: The effect of setup on overall navigation accuracy could...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 19, 2013· Ge Healthcare It

Recalled Item: Centricity Enterprise Archive is a software product for receiving Recalled...

The Issue: GE Healthcare has become aware of a potential data loss issue associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2013· OrthoPediatrics Corp

Recalled Item: 90 Degree Cannulated Infant Blade Plate 30mm x 5mm x Recalled by...

The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2013· OrthoPediatrics Corp

Recalled Item: 90 Degree Cannulated Infant Blade Plate 25mm x 5mm x Recalled by...

The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2013· OrthoPediatrics Corp

Recalled Item: 90 Degree Cannulated Infant Blade Plate 35mm x 5mm x Recalled by...

The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2013· Cook, Inc.

Recalled Item: Zilver PTX Drug-Eluting Peripheral Stent Recalled by Cook, Inc. Due to Cook...

The Issue: Cook Medical has received a small number of complaints related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 18, 2013· Cook, Inc.

Recalled Item: Zilver¿ PTX¿ Drug-Eluting Peripheral Stent - 6 mm X 80mm Recalled by Cook,...

The Issue: Cook Medical has received a small number of complaints related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 18, 2013· Carl Zeiss Meditec, Inc.

Recalled Item: Zeiss brand OPMI Pentero C Recalled by Carl Zeiss Meditec, Inc. Due to Carl...

The Issue: Carl Zeiss Meditec is conducting a field corrective action for its OPMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2013· Beckman Coulter Inc.

Recalled Item: Synchron LX System(s) and UniCel DxC 600/800 System(s) Lactate Reagent...

The Issue: Beckman Coulter initiated the recall for the Lactate Assay (LACT) Lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2013· Alcon Grieshaber AG

Recalled Item: The Constellation Vision System Pneumatic Handpiece. Indicated for both...

The Issue: Alcon is conducting a Medical Device Removal for the Constellation Pneumatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2013· Ziemer Usa Inc

Recalled Item: 1) The FEMTO LDV Z2 Femtosecond Surgical Laser is an Recalled by Ziemer Usa...

The Issue: A defect in the controller board can lead to the condenser to the video...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2013· Alere San Diego, Inc.

Recalled Item: Alere" hCG Combo Cassette (20/10 mIU/mL) Kit. Product Usage: The Recalled by...

The Issue: The firm initiated recall of Alere" hCG Combo Cassette (20/10 mIU/mL) kit PN...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2013· Bard Peripheral Vascular Inc

Recalled Item: BARD Biopsy Systems UltraClip Dual Trigger breast tissue marker. Intended...

The Issue: Bard Peripheral Vascular (BPV) has confirmed that some devices with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray systems Product Usage: The Brilliance CT 64...

The Issue: Philips Healthcare received reports from the field that certain Brilliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Medrad Inc

Recalled Item: DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris Recalled by...

The Issue: The firm is recalling these power cables due to a latent design reliability...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle InsuLinx Blood Glucose Monitoring System: For In Vitro Diagnostic...

The Issue: AT rare, extremely high glucose levels (1024 mg/dL and above), the FreeStyle...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 15, 2013· Hill-Rom, Inc.

Recalled Item: Hill-Rom 1000 Bed Recalled by Hill-Rom, Inc. Due to Complaints have been...

The Issue: Complaints have been reported for brakes disengaging when the bed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Hand Switch - Electric Pen Drive Recalled by Synthes USA HQ, Inc....

The Issue: Synthes received a complaint from a customer in which the Hand Switch for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing