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 2728127300 of 27,558 recalls

Medical DeviceOctober 28, 2011· Shimadzu Medical Systems

Recalled Item: R-30H Recalled by Shimadzu Medical Systems Due to Shimadzu is recalling...

The Issue: Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2011· Progressive Medical Inc

Recalled Item: Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm)...

The Issue: The tip of the product could come loose or unravel.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2011· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to As part of GE Innova IQ...

The Issue: As part of GE Innova IQ table introduction, a label was designed to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2011· Medtest Holdings, Inc.

Recalled Item: Pointe Scientific Liquid Creatine Kinase Reagent Set Device is a Recalled by...

The Issue: Linear performance information in product insert does not match that listed...

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

Class III — Low RiskOngoing
Medical DeviceOctober 19, 2011· Merge Healthcare, Inc.

Recalled Item: CADstream software Product Usage: CADstream is an image processing system...

The Issue: Customers may experience an issue with the software study preferences when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2011· Philips Healthcare Inc.

Recalled Item: Philips Healthcare Practix Convenio Mobile X-ray system Worldwide...

The Issue: When the system is switched off or when the tube arm is parked in the down...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2011· Exactech, Inc.

Recalled Item: OPTETRAK LOGIC Proximal Tibial Spacer & Screws (2) 2.5 LT BLUE Size 2.5...

The Issue: Exactech, Inc. of Gainesville, FL recalled their Optetrak Proximal Tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2011· SCC Soft Computer

Recalled Item: SoftLab with SA INST versions: 3.1.6.12 Recalled by SCC Soft Computer Due to...

The Issue: On 10/17/2011 SCC Soft Computer, Clearwater, FL initiated a correction on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2011· Intuitive Surgical, Inc.

Recalled Item: da Vinci Si Surgical System IS3000 with the da Vinci Recalled by Intuitive...

The Issue: Improper restraints during transportation of the da Vinci system could cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2011· Intuitive Surgical, Inc.

Recalled Item: Thyroidectomy Indication for the da Vinci Surgical Systems Recalled by...

The Issue: Promotional literature for use of the da Vinci system for thyroidectomy,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2011· Beckman Coulter Inc.

Recalled Item: UniCel DxI 600 Access Immunoassay Systems Recalled by Beckman Coulter Inc....

The Issue: The recall was initiated because Beckman Coulter has received seven reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2011· Beckman Coulter Inc.

Recalled Item: UniCel DxC 660i Recalled by Beckman Coulter Inc. Due to The recall was...

The Issue: The recall was initiated because Beckman Coulter has received seven reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2011· Beckman Coulter Inc.

Recalled Item: UniCel DxI 800 Access Immunoassay Systems Recalled by Beckman Coulter Inc....

The Issue: The recall was initiated because Beckman Coulter has received seven reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2011· Beckman Coulter Inc.

Recalled Item: Access Total T3 Reagent Recalled by Beckman Coulter Inc. Due to A recall was...

The Issue: A recall was initiated because Beckman Coulter has identified a negative...

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

Class III — Low RiskOngoing
Medical DeviceOctober 10, 2011· RAYSEARCH LABORATORIES AB

Recalled Item: SharePlan 1.1 Recalled by RAYSEARCH LABORATORIES AB Due to This notice...

The Issue: This notice concerns behavior of the SharePlan that may be unexpected and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2011· Orthosoft, Inc. dba Zimmer CAS

Recalled Item: Navitrack System - OS Knee Universal Recalled by Orthosoft, Inc. dba Zimmer...

The Issue: Zimmer CAS voluntarily conducted a retrospective recall of the Navitrack...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2011· Custom Medical Specialties, Inc.

Recalled Item: CMS-2890 Custom Needle Local Tray containing PVP Prep Pad The Recalled by...

The Issue: The firm saw on the FDA web site a recall by the manufacturer due to no...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2011· Custom Medical Specialties, Inc.

Recalled Item: CMS-8457 Hysteroscopic Sterilization Pack containing 4 oz. bottle PVP Prep...

The Issue: The firm saw on the FDA web site a recall by the manufacturer of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2011· Custom Medical Specialties, Inc.

Recalled Item: CMS-2586 Custom Amnio Tray containing 2 oz. bottle PVP Prep Recalled by...

The Issue: The firm saw on the FDA web site a recall by the manufacturer of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2011· Custom Medical Specialties, Inc.

Recalled Item: CMS-4316 Custom Vein Tray containing 4 oz. bottle PVP Prep Recalled by...

The Issue: The firm saw on the FDA web site a recall by the manufacturer of the...

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

Class I — Serious Health HazardOngoing