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 2712127140 of 27,558 recalls

Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Secondary VSA Set Peristaltic Pump...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion Pump Peristaltic Pump System designed for...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Secondary Set Peristaltic Pump System...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Side Step Set Peristaltic Pump...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2012· ICU Medical, Inc.

Recalled Item: High Pressure Stopcock (3-Way Recalled by ICU Medical, Inc. Due to The firm...

The Issue: The firm initiated the recall due to a molding defect in a high pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2012· ICU Medical, Inc.

Recalled Item: 94" (239cm) 20 Drop Admin Set w/High Pressure 4-Way (300 psi) Stopcock...

The Issue: The firm initiated the recall due to a molding defect in a high pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2012· ICU Medical, Inc.

Recalled Item: Flush Kit w 3 Way Off Stopcock Product Usage: Flush Kit Recalled by ICU...

The Issue: The firm initiated the recall due to a molding defect in a high pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2012· ICU Medical, Inc.

Recalled Item: Cardiac Catheterization Waste Management System w/1000mL Waste Bag Recalled...

The Issue: The firm initiated the recall due to a molding defect in a high pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2012· Berchtold Corp.

Recalled Item: OPERON D850 Surgical Table Product Usage: Surgical Table Recalled by...

The Issue: Table was not lowering.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2012· Maquet Medical Systems, Usa

Recalled Item: Maquet Getinge Group Operating Table System Magnus Carbon-Fibre Table Top...

The Issue: As a result of a small number of customer complaints, MAQUET conducted an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2012· Becton Dickinson & Co.

Recalled Item: Gram Crystal Violet 250 mL Recalled by Becton Dickinson & Co. Due to...

The Issue: Potential for increase level of artifacts to appear as large, spherical and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2012· Becton Dickinson & Co.

Recalled Item: BD Gram Stain Kit Recalled by Becton Dickinson & Co. Due to Potential for...

The Issue: Potential for increase level of artifacts to appear as large, spherical and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2012· Varian Medical Systems, Inc.

Recalled Item: Rectal Retractors Recalled by Varian Medical Systems, Inc. Due to A medical...

The Issue: A medical device used in brachytherapy may become contaminated and can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2012· Varian Medical Systems, Inc.

Recalled Item: Rectal Retractors Recalled by Varian Medical Systems, Inc. Due to A medical...

The Issue: A medical device used in brachytherapy may become contaminated and can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: E.CAM emission computed tomography system used to detect or image Recalled...

The Issue: Radial motor drives replaced during a customer service action were...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia E is a multi-purpose SPECT system used to detect Recalled by Siemens...

The Issue: Radial motor drives replaced during a customer service action were...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2012· Beckman Coulter Inc.

Recalled Item: AutoMate 1250 and AutoMate 2550 Recalled by Beckman Coulter Inc. Due to The...

The Issue: The recall was initiated because Beckman Coulter has confirmed customer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 10, 2012· Kerr Corporation

Recalled Item: The brand name of the device is Laser Loupes Recalled by Kerr Corporation...

The Issue: The firm initiated the recall for Laser Loupes because the ink used to mark...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***All in one CrossFT***Punch***PFT-00M***4.5mm to 6.5mm***CONMED LINVATEC...

The Issue: ConMed Linvatec is recalling the product due to the punch being...

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

Class II — Potential Health HazardOngoing