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. 1,740 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,740 in last 12 months

Showing 3414134160 of 47,632 recalls

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· 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 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· 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· 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· 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 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: Gold-Tite Hexed Retaining Screw 3mm Item: GSH30 Dental implants Recalled by...

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: Certain EP Healing Abutment 5mm(D) x 5.6mm(P) x 2mm(H) Item: Recalled by...

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: Certain Pick-Up Coping 5mm(D) x 5mm(P) Item:IWIP55 Dental implants Recalled...

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: Standard Abutment Temporary Screw 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: Standard Abutment Transfer Coping 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: Preformance 15 degrees pre-angled post Dental implants Recalled by Biomet...

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: Certain Temporary Non-Hexed 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
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: LDA Screw SBL 4mm(D) Item: SCRSBL2 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
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
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Gingihue 15 degree Angled Post 4.1mm(D) x 5mm(P) x Recalled by...

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: Standard Abutment 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: 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: Conical Abutment Pick-up Coping 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