Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,535 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,535 in last 12 months

Showing 1760117620 of 28,355 recalls

Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS MISS/MIS Poly Screw Driver. Part of MAXIMIS Pedicle...

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 40mm 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 Poly Screw 5.5 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 Poly Screw 6.5 x 40mm. 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 Extension Sleeve. Part of MAXIMIS Pedicle Screw Spinal...

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 Persuader. Part of MAXIMIS Pedicle Screw Spinal Fixation...

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 Tapper 6.5. Part of MAXIMIS Pedicle Screw Spinal 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 45mm 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 Reduction B. Part of MAXIMIS Pedicle Screw Spinal 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 Poly Screw 5.5 x 50mm and 5.5 x 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 Rod Pusher Angled. 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 S. Probe. 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 250mm 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 MIS Screw 6.5 x 50mm and 6.5 x Recalled by Valorem Surgical...

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 Reduction A. Part of MAXIMIS Pedicle Screw Spinal 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 Poly Screw 5.5 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 Extension Driver. Part of MAXIMIS Pedicle Screw Spinal...

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 30 mm Curved Rod. Part of MAXIMIS Pedicle 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 Driver. 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 45mm MIS . 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