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 2070120720 of 27,558 recalls

Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Preformance Temporary Cylinder 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: Bellatek Encode Healing 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: Cover Screw Dental implants Recalled by Biomet 3i, LLC Due to Pouches may...

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 24, 2015· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System. Used to manage workflows for treatment...

The Issue: First Databank (FDB) is a third party product incorporated into MOSAIQ. FDB...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· Intuitive Surgical, Inc.

Recalled Item: 0 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...

The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· Intuitive Surgical, Inc.

Recalled Item: 30 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...

The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· ZYTO Technologies, Inc.

Recalled Item: The ZYTO Tower is the input device to program the Recalled by ZYTO...

The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Cournand Modified 2-PC 19G Recalled by Stryker Instruments Div. of Stryker...

The Issue: The Guidewire Introducer Needle (0910-192-000) was shipped after the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2015· ZYTO Technologies, Inc.

Recalled Item: The ZYTO Select and ZYTO Elite software programs are used Recalled by ZYTO...

The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· Steris Corporation

Recalled Item: AMSCO¿ Warming Cabinet. Manufactured by: STERIS Corporation To raise the...

The Issue: The firm discovered that information printed on the quick magnet is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· Biomet, Inc.

Recalled Item: A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization...

The Issue: These screws have a single lead (instead of a triple lead) thread. The screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· Boston Scientific Corp

Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-8 Material Number:...

The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· Bigwall Enterprises

Recalled Item: WARM STEAM Personal Steam Inhaler-Adjustable control to regulate flow of...

The Issue: "The public reason for the recall is that the product is being recalled out...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· Boston Scientific Corp

Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 OUS Recalled by...

The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· Boston Scientific Corp

Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve Recalled by Boston Scientific Corp...

The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· Boston Scientific Corp

Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 Recalled by Boston...

The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2015· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is voluntarily recalling its Chariot" Guiding Sheath. To...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 - Foam of 100 tests WW. Recalled by Biomerieux...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 -pack of 30 tests US. Etest¿ Recalled by...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing