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. 2,448 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,448 in last 12 months

Showing 1980119820 of 27,462 recalls

Medical DeviceMarch 15, 2016· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare System X-ray Tomography Computed : Recalled by Philips...

The Issue: It was discovered the patient support tabletop may fail to move in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Bariatric Bed w/o mattress & rails Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Ventlab LLC

Recalled Item: STAT-Check Resuscitation Bag Manual Emergency Resuscitation Bag with Carbon...

The Issue: Stat-check CO2 indicators are non-functional. The indicator is yellow when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Bariatric Bed with mattress and rails Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare System X-ray Tomography Computed : Recalled by Philips...

The Issue: It was discovered the patient support tabletop may fail to move in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA Duodenovideoscope Olympus TJF Type 160F/VF used with an Recalled...

The Issue: New reprocessing instructions for the Olympus TJF-160/VF duodenoscopes,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Junction Boxes Recalled by Invacare Corporation Due to The firm recently...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Invacare Corporation

Recalled Item: Invacare¿ Foot Section for Semi & Full Electric Beds Recalled by Invacare...

The Issue: The firm recently identified a quality issue with the Junction box used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 for Proton Radiation Therapy Recalled by Mevion Medical Systems,...

The Issue: Possibility of Gantry Motion with Aperture or Compensator only partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Vaxcel PICC with PASV IR-145 Kit under the following labels: 1) 4F Recalled...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood Parameter Monitoring System 500 Cardiopulmonary bypass on-line...

The Issue: Specific CDI¿ Blood Parameter Monitoring System 500 devices are being...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Ossur H / F

Recalled Item: Ossur Lil Angel Vest P3 Kodel. Pediatric sized vest is Recalled by Ossur H /...

The Issue: There is a potential for partial or complete fracture of the plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Ossur H / F

Recalled Item: Ossur Lil Angel Vest P2 Lambswool. Pediatric sized vest is Recalled by Ossur...

The Issue: There is a potential for partial or complete fracture of the plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Ossur H / F

Recalled Item: Ossur Lil Angel Vest P2 Sorbatex. Pediatric sized vest is Recalled by Ossur...

The Issue: There is a potential for partial or complete fracture of the plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Xcela PICC with PASV Valve Technology Recalled by Navilyst Medical, Inc., an...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Ossur H / F

Recalled Item: Ossur Lil Angel Vest P2 Kodel. Pediatric sized vest is Recalled by Ossur H /...

The Issue: There is a potential for partial or complete fracture of the plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Vaxcel PICC with PASV Catheter Kit under the following labels: 1) 3F...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Vaxcel PICC with PASV Introducer Kit under the following labels: 1) 4F...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Xcela PICC with PASV Valve Technology Catheter Kit Recalled by Navilyst...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

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

Class II — Potential Health HazardOngoing