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. 2,330 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,330 in last 12 months

Showing 3944139460 of 48,219 recalls

Medical DeviceSeptember 23, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego systems Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A cable inside the C-arm systems may have been routed in an inappropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2014· Virtual Imaging, Inc.

Recalled Item: Digital Mobile X-ray Systems used to take diagnostic radiographic exposures...

The Issue: There is a potential for unintended and erratic motion.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Carescape Patient Data Module Recalled by GE Healthcare, LLC...

The Issue: GE Healthcare has recently become aware of a potential safety issue to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: External power supply adaptors that accompany Clinitek Status Connect System...

The Issue: The external power supply for the Clintek Status analyzer, which is provided...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: External power supply adaptors that accompany Clinitek Status+ The Clinitek...

The Issue: The external power supply for the Clintek Status analyzer, which is provided...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· Siemens Healthcare Diagnostics

Recalled Item: IMMULITE /IMMULITE 1000 Systems COR Cortisol Recalled by Siemens Healthcare...

The Issue: Customer complaints were received for positive bias reported on the controls...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: External power supply adaptors that accompany Clinitek Status Power Supply...

The Issue: The external power supply for the Clintek Status analyzer, which is provided...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number:...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number:...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: MediChoice¿ Multifunction Electrode Part Number: MC171 OH Recalled by...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Intuitive Surgical, Inc.

Recalled Item: EndoWrist Stapler 45 instrument for the da Vinci Si System Recalled by...

The Issue: Intuitive is issuing an urgent product notice to all users of the EndoWrist...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A Recalled...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
DrugSeptember 18, 2014· Bracco Diagnostic Inc

Recalled Item: E-Z- GAS II EFFERVESCENT GRANULES Antacid/Antiflatulent Recalled by Bracco...

The Issue: Subpotent Drug: Out of Specification (OOS) result during routine stability...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 17, 2014· Janssen Ortho L.L.C.

Recalled Item: Xarelto (rivaroxaban) Tablets 15 mg per tablet Recalled by Janssen Ortho...

The Issue: Microbial Contamination of Non-Sterile Products: Consumer complaint...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Richard-Allan Scientific Specimen Transportation System. 10% NBF is used to...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Richard-Allan Scientific 10% Neutral Buffered Formalin. Product Usage: 10%...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Richard-Allan Scientific Specimen Transportation System. Product Usage: 10%...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Cardinal Health Prefilled Buffered 10% Formalin. Product Usage:10% NBF is...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing