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. 2,404 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,404 in last 12 months

Showing 2292122940 of 27,462 recalls

Medical DeviceAugust 14, 2014· The Anspach Effort, Inc.

Recalled Item: Synthes Small Electric Drive (SED). For use in general traumatology....

The Issue: The affected Small Electric Drive (SED) may operate solely in reverse mode,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2014· Sam Medical Products

Recalled Item: SAM Junctional Tourniquet (SJT) Auxiliary Recalled by Sam Medical Products...

The Issue: SAM Junctional Tourniquet (SJT) Auxiliary strap, model SJT 102 and SJT 112,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ HbA1c Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: In March, Siemens Healthcare Diagnostics issued an Urgent Medical Device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ Negative Pressure Wound Therapy (NPWT) System (RENASYS EZ)...

The Issue: Modification were made to the RENASYS EZ NPWT Systems without a 510(k) or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Biofire Defense

Recalled Item: JBAIDS Instrument System Software version 3.5.0.72. The JBAIDS instrument is...

The Issue: BioFire Defense, LLC is initiating a field action for JBAIDS Software...

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Water may leak...

The Issue: Water may leak into the center gas lumen of the Patient Circuit

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Centaur XP Immunoassay System Recalled by Siemens Healthcare...

The Issue: The firm is conducting a field correction for the ADVIA Centaur and ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Maquet Cardiovascular, LLC

Recalled Item: Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump...

The Issue: An internal finding identified the presence of pinholes/cuts in some of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: V5Ms Transesophageal transducers Recalled by Siemens Medical Solutions USA,...

The Issue: Reports of deterioration of material covering the articulating section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Centaur Immunoassay System Recalled by Siemens Healthcare Diagnostics...

The Issue: The firm is conducting a field correction for the ADVIA Centaur and ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Volcano Corporation

Recalled Item: Volcano TrakBack II Disposable Pullback Device Recalled by Volcano...

The Issue: Internal testing had identified a potential breach to the sterile barrier...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2014· Gendex Corp

Recalled Item: eXpertDC intraoral x-ray Recalled by Gendex Corp Due to Two (2) failures of...

The Issue: Two (2) failures of the spring link components within the articulated arm...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Luminos dRF system with SW VD10 or on Luminos Recalled by Siemens...

The Issue: It was determined that a potential malfunction may occur on the Luminos dRF...

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

Class II — Potential Health HazardOngoing