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. 2,378 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,378 in last 12 months

Showing 2532125340 of 27,462 recalls

Medical DeviceMay 7, 2013· SpineFrontier, Inc.

Recalled Item: InSpan Inserter Recalled by SpineFrontier, Inc. Due to Potential for set...

The Issue: Potential for set screw to be come deformed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2013· Zimmer Surgical Inc

Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...

The Issue: This removal is in response to complaints alleging that the Zimmer Air...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2013· Zimmer Surgical Inc

Recalled Item: The Zimmer Air Dermatome Recalled by Zimmer Surgical Inc Due to This removal...

The Issue: This removal is in response to complaints alleging that the Zimmer Air...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2013· Zimmer Surgical Inc

Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...

The Issue: This removal is in response to complaints alleging that the Zimmer Air...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Long Recalled...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Trocar With (2) Fixation Cannulae - 5mm Recalled...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...

The Issue: There is evidence that an electrical short within the systems connector has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci 5 mm Instrument Cannulae for use with the Recalled by Intuitive...

The Issue: Intuitive Surgical is implementing a voluntary Field Action to implement a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Alphatec Spine, Inc.

Recalled Item: Leucadia Autolok" Polyaxial Pedicle Screw System. Intended to help provide...

The Issue: Alphatec Spine initiated this medical device recall for the following...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Product...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens RAD Fluoro Uro Systems - Luminos dRF Recalled by Siemens Medical...

The Issue: Siemens has discovered through product monitoring a potential malfunction...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach MIA 16 (16cm Minimally Invasive Attachment) Recalled by The Anspach...

The Issue: Product did not reach expected sterility assurance level

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: 1) VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to There is evidence...

The Issue: There is evidence that an electrical short within the systems connector has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Short...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: ORTHO¿ Assay Software (OAS) Server Recalled by Ortho-Clinical Diagnostics...

The Issue: There is evidence that an electrical short within the systems connector has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System (product code 6802413) Product Usage: For...

The Issue: There is evidence that an electrical short within the systems connector has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Fixation Cannula - 5mm Product Code: ONBFCA5ST...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci 5 mm Flared Instrument Cannulae for use with Recalled by Intuitive...

The Issue: Intuitive Surgical is implementing a voluntary Field Action to implement a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Fixation Cannula - 5mm Short Product Code:...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System (product code 6802783) Product Usage:...

The Issue: There is evidence that an electrical short within the systems connector has...

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

Class II — Potential Health HazardOngoing