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 2738127400 of 27,558 recalls

Medical DeviceMarch 16, 2011· Hospira Inc.

Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to May go to a white...

The Issue: May go to a white screen due to a problem with the SOM2 module. A white...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2011· Biomet Spine LLC.

Recalled Item: LANX Recalled by Biomet Spine LLC. Due to Biomet Spine, LLC. announces...

The Issue: Biomet Spine, LLC. announces voluntary recall of Durango Anchored ALIF Plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2011· The Anspach Effort, Inc.

Recalled Item: ****** 3mm Diamond Ball. Used for cutting and shaping bone. Recalled by The...

The Issue: Due to three batches of product may have diamond grit size larger than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2011· Ge Healthcare It

Recalled Item: Imagecast PACS is an image management system intended to be Recalled by Ge...

The Issue: In Imagecast PACS versions prior to 3.6.51.01, the estimated magnification...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2011· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-Ray System Recalled by Philips Medical...

The Issue: Multiple software defects which could impact the performance or reliability...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardioplegia Delivery Set - Heat Exchanger Cardiopulmonary...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardioplegia Delivery Sets Catalog Code: 204880 Product Usage:...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular and Perfusion Procedure Kits Catalog Codes:...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardioplegia Delivery Set- Catalog Number:165720 and Catalog...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Integrated Cardioplegia Delivery Set-LINE FOR 15501/16015/5852...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Cardioplegia Delivery Set- Item Number: 16130 Product Usage: The...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2011· Primus Medical LLC

Recalled Item: AC Powered adjustable hospital bed Recalled by Primus Medical LLC Due to The...

The Issue: The "Retaining washers & Clevis Pins" provided with the AC -powered...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit Recalled by...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit Recalled by...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Nemschoff Chairs, Inc.

Recalled Item: Nemschooff Recalled by Nemschoff Chairs, Inc. Due to Nemschoff Chairs, Inc....

The Issue: Nemschoff Chairs, Inc. is recalling various model of the Serenity Treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit Recalled by...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit Recalled by...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing