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. 2,461 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,461 in last 12 months

Showing 1842118440 of 27,462 recalls

Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: IWS Infant Warmer System-Infant radiant warmers provide infrared heat...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Incubator The Giraffe Incubator is an infant incubator. Incubators...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Spot PT Ohmeda Medical Spot PT Lite Phototherapy System- Recalled by...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe OmniBed Ohmeda Medical Giraffe OmniBed- The OmniBed is a Recalled by...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Bedded Warmer Recalled by Ohmeda Medical Due to Certain power cords...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Bedded Warmer Recalled by Ohmeda Medical Due to Certain power cords...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: CarePlus Incubator Ohmeda-Ohio CarePlus Incubator- Incubators provide a...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Incubator Ohmeda Medical Giraffe Incubator-The Giraffe Incubator is...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Bedded Warmer Recalled by Ohmeda Medical Due to Certain power cords...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Teleflex Medical

Recalled Item: WECK Visistat 35W Recalled by Teleflex Medical Due to Sterility Deficiency:...

The Issue: Sterility Deficiency: The packages are not sealed properly and thus the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: FV-RF (Clinix RF Plus) Product Usage: A Stationary X-ray System Recalled by...

The Issue: There's a potential for liquid penetration into the back side of the front...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Swissray Medical

Recalled Item: ddR Formula B X-ray System Recalled by Swissray Medical Due to Potential for...

The Issue: Potential for bucky (the part that holds the grid and is moveable to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2016· Ultradent Products, Inc.

Recalled Item: UltraSeal XT Plus Clear . The package contains 4x 1.2 Recalled by Ultradent...

The Issue: There was a labeling error with product, UltraSeal XT Plus Clear , Part...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2016· Teleflex Medical

Recalled Item: Weck Facial Closure Systems have application in laparoscopic procedures for...

The Issue: The devices wings may become partially detached from the EFx Shield during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2016· Smith & Nephew, Inc.

Recalled Item: (R) DEAD BLOW MALLET Recalled by Smith & Nephew, Inc. Due to The firm...

The Issue: The firm received complaints of cracks in the weld on the head of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2016· Medtronic Inc

Recalled Item: Affinity Fusion" Oxygenator with Integrated Arterial Filter Recalled by...

The Issue: Medtronic is initiating a voluntary product recall for specific lot numbers...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2016· Roche Molecular Systems, Inc.

Recalled Item: LightMix¿ Zika rRT-PCR Test The LightMix¿ Zika rRT-PCR Test is Recalled by...

The Issue: The LightCycler¿ 480 algorithm used for the LightMix¿ Zika rRT-PCR Test, EUA...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Smith & Nephew, Inc.

Recalled Item: Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...

The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Smith & Nephew, Inc.

Recalled Item: Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...

The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash System Recalled by Siemens Medical Solutions USA,...

The Issue: Software update that provides software and firmware bug-fixes to improve...

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

Class II — Potential Health HazardOngoing