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 1720117220 of 27,558 recalls

Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS MISS/MIS Compressor and Rod Tightener. Part of MAXIMIS...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS MIS Poly Screw Driver B. Part of MAXIMIS Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS MIS Screw 6.5 x 55mm. Part of MAXIMIS Recalled by Valorem...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 55mm MIS Rod. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 60mm Curved Rod. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Contiplex Nerve Block Tray. Product Catalog Number: 570205. Local anesthesia...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Poly Screw 6.5 x 45mm. Part of MAXIMIS Recalled by Valorem...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Ratchet T Handle. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Poly Screw 6.5 x 50mm. Part of MAXIMIS Recalled by Valorem...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Dilator A. Part of MAXIMIS Pedicle Screw Spinal Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 35mm Rod. Part of MAXIMIS Pedicle Screw Spinal Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 50mm MIS Rod. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 30mm Rod. Part of MAXIMIS Pedicle Screw Spinal Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Rod Pusher B. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 80mm MIS Rod. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Polyaxial and MIS Screw Recalled by Valorem Surgical LLC...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 80mm Straight Rod. Part of MAXIMIS Pedicle Screw Recalled...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 60mm Curved and Precontoured Rod. Part of MAXIMIS Recalled...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 50mm Curved Rod. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Poly Screw 7.5 x 45mm. Part of MAXIMIS Recalled by Valorem...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing