Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,367 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,367 in last 12 months

Showing 2740127420 of 27,462 recalls

Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Loop Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2009· Alere San Diego, Inc.

Recalled Item: Triage TOX Drug Screen Panel Recalled by Alere San Diego, Inc. Due to...

The Issue: Biosite is recalling the Triage TOX Drug Screen kits where the box...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2009· Sunquest Information Systems, Inc.

Recalled Item: Sunquest Encompass The reporting site is using the Encompass software...

The Issue: Sunquest is recalling the Sunquest Encompass versions 2.4 and later because...

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

Class III — Low RiskOngoing
Medical DeviceApril 6, 2009· Stellate Systems

Recalled Item: Harmonie software versions 5.1 uo to 6.2e : Harmonie-E Long Recalled by...

The Issue: The firm is initiating this recall because the implied or stated indications...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2009· Invatec Llc

Recalled Item: lnvatec SpA brand Diver C.E. Recalled by Invatec Llc Due to Devices labeled...

The Issue: Devices labeled for an intended use was not included in the existing 510(k)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2009· Zynex Medical, Inc.

Recalled Item: IF 8000 Recalled by Zynex Medical, Inc. Due to Zynex notified customers that...

The Issue: Zynex notified customers that a malfunction in the IF 8000 can result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 5.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 5.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 5.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 5.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing