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. 2,442 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,442 in last 12 months

Showing 1850118520 of 27,558 recalls

Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: K-Wire 1.4mm x 12in Non-Threaded Recalled by Amendia, Inc Due to The rods...

The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Teleflex Medical

Recalled Item: RUSCH Recalled by Teleflex Medical Due to Labeling Inconsistency: The...

The Issue: Labeling Inconsistency: The products have been labeled with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Black Widow 6.6mm x 20mm Screw Recalled by Amendia, Inc Due to There is a...

The Issue: There is a problem with the mating feature between the plate and screw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Savannah-T Straight Rod Recalled by Amendia, Inc Due to The rods are...

The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Interventional Spine Inc

Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...

The Issue: During implantation, the proximal end of the device could separate if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Perspective Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens is providing a new installation of the Residual Current Monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestilix Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestige II Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: SFX Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting a...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: ADVANTX LCN+ Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: ADVANTX LCLP+ Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Legacy Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting a...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Innova 2000 Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: ADVANTX LCV+ Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: RFX Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting a...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestige SI Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: ADVANTX LCA Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Precision 500D Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestige VH Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· Tepha Incorporated

Recalled Item: GalaSHAPE 3D Recalled by Tepha Incorporated Due to Endotoxin values from...

The Issue: Endotoxin values from testing of retains slightly exceeded the established...

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

Class II — Potential Health HazardOngoing