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 2632126340 of 27,462 recalls

Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Brivo XR 285 Mobile general purpose radiographic imaging...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA ML Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...

The Issue: Horiba Medical is recalling ABX PENTRA ML because they have confirmed an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 200amx with digital upgrade Mobile general Recalled...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 220amx Mobile general purpose radiographic imaging...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: Sorin C5 Perfusion System Recalled by Sorin Group USA, Inc. Due to Sorin...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Trumpf Medical Systems, Inc.

Recalled Item: Helion and Xenion surgical lights Recalled by Trumpf Medical Systems, Inc....

The Issue: Incidents regarding fractures of the front joint of the spring arm have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: S5 Mast Roller Pump 150 Recalled by Sorin Group USA, Inc. Due to Sorin Group...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: S5 Single Roller Pump 150 Recalled by Sorin Group USA, Inc. Due to Sorin...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: S5 Double Roller Pump 85 Recalled by Sorin Group USA, Inc. Due to Sorin...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: S5 Mast Roller Pump 85 Recalled by Sorin Group USA, Inc. Due to Sorin Group...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Cure Medical LLC

Recalled Item: Male Recalled by Cure Medical LLC Due to The firm initiated the product...

The Issue: The firm initiated the product recall because labeling on some of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental Kodak 2200 Intraoral X-ray system Product Usage: The...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental CS 2100 X-ray system Product Usage: The expected Recalled...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental Kodak 2100 Intraoral X-ray system Product Usage: The...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Instratek, Incorporated

Recalled Item: Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The...

The Issue: Instratek, Inc.has received multiple complaints of the 1052 Trigger Finger...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by...

The Issue: The low contrast pins in the Image Quality (IQ) phantom deteriorates over...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Iris Diagnostics

Recalled Item: Iris Diagnostics Division iQ Control/Focus Set Recalled by Iris Diagnostics...

The Issue: The firm initiated this recall because complaints from customers reported...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Elekta, Inc.

Recalled Item: MOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR)...

The Issue: A patient was seriously mistreated after a user made and saved an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental CS 2200 X-ray system Product Usage: The expected Recalled...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDLab¿ 1260 system blood gas analyzer Product Usage: RAPIDLab...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing