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 2210122120 of 27,462 recalls

Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Xper cardio systems Model : 722123 Product Usage:...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Allure BiPlane Series: Model 722013 Allura Xper FD20...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare INTEGRIS vascular System Model : 722122 Product Usage:...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Synthes, Inc.

Recalled Item: Synthes Inserter for Titanium Elastic Nails Recalled by Synthes, Inc. Due to...

The Issue: The Inserter has the potential for mechanical failures such as breakage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Allura Xper Series: Allura Xper FD10 Allura Xper Recalled...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare INTEGRIS H5000F/Allura 9F Model : 722017 Product Usage:...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2015· Bradshaw Medical Inc.

Recalled Item: Axial Torque Limiting Driver (1st generation) Product Usage: The Bradshaw...

The Issue: A component failure could cause a situation where the applied torque was...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2015· Invacare Corporation

Recalled Item: Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair) Recalled by...

The Issue: The batteries used in the Invacare¿ Pronto¿ Air Personal Transporter models...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2015· Smiths Medical ASD, Inc.

Recalled Item: CADD" Medication Cassette Reservoir Recalled by Smiths Medical ASD, Inc. Due...

The Issue: Smiths Medical has become aware of an issue with specific lots of 50mL CADD"...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2015· Penner Mfg Inc

Recalled Item: Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1...

The Issue: If the patient sits on either wing, not squarely on the center section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2015· C.R. Bard, Inc.

Recalled Item: Bard 100% Latex-Free Urinary Drainage Bag with Anti- Chamber and Recalled by...

The Issue: Potential breach of the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2015· GE Healthcare

Recalled Item: GE Healthcare Proteus XR/a with wall stand model number 2260354. Recalled by...

The Issue: Potential breakage of the steel cable which supports the bucky device in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2015· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...

The Issue: Power supply malfunction complaints related to suboptimal thermal management.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2015· Elekta, Inc.

Recalled Item: Elekta Precise Treatment Table Recalled by Elekta, Inc. Due to It is...

The Issue: It is possible to position the Treatment Table with errors greater than 5mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2015· Medical Components, Inc dba MedComp

Recalled Item: 9F Plastic Dual Port Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: The dual port with catheters was not covered under FDA clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...

The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· GE Healthcare

Recalled Item: GE Healthcare Engstrom Carestation Recalled by GE Healthcare Due to...

The Issue: Potential failure of the caster mounting hardware, which may result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...

The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...

The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2015· CooperSurgical, Inc.

Recalled Item: NovaPlus Brand Warm Gel Infant Heel Gel Warmer Recalled by CooperSurgical,...

The Issue: Products without expiration date have the remote potential for minor burn

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

Class II — Potential Health HazardOngoing