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. 2,396 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,396 in last 12 months

Showing 2056120580 of 27,558 recalls

Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 20 Recalled by Beckman Coulter...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 21 Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 23 Recalled by Beckman Coulter...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Microbiologics Inc

Recalled Item: QC Sets and Panels: KWIK-STIK Cepheid Smart GBS QC Set Recalled by...

The Issue: The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Microbiologics Inc

Recalled Item: QC Sets and Panels: KWIK-STIK. Cepheid Xpert GBS QC Set Recalled by...

The Issue: The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Baxter Healthcare Corp.

Recalled Item: Baxter INTERLINK System Recalled by Baxter Healthcare Corp. Due to Potential...

The Issue: Potential for dark loose particulate matter (400 microns or smaller) on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Verathon, Inc.

Recalled Item: GlideScope AVL Video Laryngoscope (AVL) Recalled by Verathon, Inc. Due to...

The Issue: Certain models and serial numbers of GlideScope GVL and AVL laryngoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Baxter Healthcare Corp.

Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corp. Due to Potential...

The Issue: Potential for dark loose particulate matter (400 microns or smaller) on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Aesculap, Inc.

Recalled Item: Columbus Revision Knee System Recalled by Aesculap, Inc. Due to Aesculap...

The Issue: Aesculap Inc. US has initiated a recall on Tibial and Femur extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Bayer Healthcare

Recalled Item: Medrad Source Administration Sets Recalled by Bayer Healthcare Due to The...

The Issue: The firm's investigation of the Medrad Intego indicates that the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Verathon, Inc.

Recalled Item: BladderScan BVI 9600 Recalled by Verathon, Inc. Due to The firm is providing...

The Issue: The firm is providing customers with an updated Operations and Maintenance...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Verathon, Inc.

Recalled Item: GlideScope Video Laryngoscope (GVL) Recalled by Verathon, Inc. Due to...

The Issue: Certain models and serial numbers of GlideScope GVL and AVL laryngoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Baxter Healthcare Corp.

Recalled Item: Baxter Y-Type Spike Adapter Recalled by Baxter Healthcare Corp. Due to...

The Issue: Potential for dark loose particulate matter (400 microns or smaller) on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Acumedia Manufacturers, Inc.

Recalled Item: Palcam Supplement Acumedia PN 7987 Product Usage: PALCAM Supplement is...

The Issue: Contamination of product with possible Bacillus spp

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2015· Leica Microsystems, Inc.

Recalled Item: Bond Polymer Red Detection DS9390 kits. The common name Recalled by Leica...

The Issue: The Firm informed the importer/distributor, Leica Microsystems, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Conical 25 degree Angled Abutment Dental implants Recalled by Biomet 3i, LLC...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Quickbridge TM Cap Dental implants Recalled by Biomet 3i, LLC Due to Pouches...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Temporary Healing Retention Cylinder Dental implants Recalled by Biomet 3i,...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing