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. 2,447 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,447 in last 12 months

Showing 1792117940 of 27,558 recalls

Medical DeviceMarch 23, 2017· Sysmex America Inc

Recalled Item: Sysmex Recalled by Sysmex America Inc Due to Reported customer complaints of...

The Issue: Reported customer complaints of automated hematology analyzers catching fire...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· ReFlow Medical

Recalled Item: Wingman 35 Crossing Catheter Recalled by Medical Due to Medical is recalling...

The Issue: Medical is recalling the Wingman 35 Crossing Catheter because it may be...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX Recalled by Zimmer...

The Issue: pegs shearing post-operatively

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Philips Electronics North America Corporation

Recalled Item: The following systems are only affected if a Laird chiller Recalled by...

The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Philips Electronics North America Corporation

Recalled Item: Allura Xper Release 8.2 (Laird chiller is always installed) Recalled by...

The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Philips Electronics North America Corporation

Recalled Item: UNIQ: UNIQ FD10 722026 Recalled by Philips Electronics North America...

The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Cook Medical Incorporated

Recalled Item: Zenith Alpha Thoracic Endovascular Graft The Zenith Alpha" Thoracic...

The Issue: There have been five reports of graft thrombosis/occlusion during global...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 22, 2017· Tosoh Bioscience Inc

Recalled Item: AIA-360 Analyzer is capable of performing two methods of immunoassay:...

The Issue: The firm has become aware of a potential issue with the AIA-360 analyzer...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2017· Roche Diagnostics Corporation

Recalled Item: Sample probes associated with: cobas 6000 Series System Recalled by Roche...

The Issue: Due to a design change in 2015, corrosion on the sample probe electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology The ArrowEVOLUTION Pressure...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Pressure injectable Jugular Axillo-Subclavian Central CThe CG+Arrow JACC...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow¿ VPS¿ Access Kit with Maximal Barrier Precautions for use Recalled by...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features The Arrow¿...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arterial Catheterization Kit The Arrow¿ Arterial Catheterization device...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally Recalled by Arrow...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow(R) VPS(R) Access Kit for use with 5 Fr. Peripherally Recalled by Arrow...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access Kit for use...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing