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. 2,383 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,383 in last 12 months

Showing 2436124380 of 27,462 recalls

Medical DeviceOctober 31, 2013· Hospira Inc.

Recalled Item: Hospira Acclaim Encore Infusion Pump Designed to deliver parenteral...

The Issue: Broken door assemblies on the Hospira/Abbott Acclaim Encore infusion pumps....

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 31, 2013· Hospira Inc.

Recalled Item: Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions...

The Issue: Hospira has received customer reports of broken door assemblies on the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 31, 2013· Zimmer, Inc.

Recalled Item: NexGen¿ Complete Knee Solutions Stemmed Tibial Component Precoat NexGen...

The Issue: Two complaints were received in which it was reported that the stem would...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2013· Ergosafe Products LLC DBA Prism Medical Services USA

Recalled Item: Medcare Products Max-500 Stand-N-Weigh Recalled by Ergosafe Products LLC DBA...

The Issue: The lift might fail with the labeled 500-lb. load rating.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2013· Ergosafe Products LLC DBA Prism Medical Services USA

Recalled Item: Medcare Products Max-500 Stand Recalled by Ergosafe Products LLC DBA Prism...

The Issue: The lift might fail with the labeled 500-lb. load rating.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2013· Philips Medical Systems, Inc.

Recalled Item: Easy Diagnost Eleva Universal Fluoroscopic applications Recalled by Philips...

The Issue: The delivered application software was an outdated version to the model of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2013· Maquet Cardiovascular, LLC

Recalled Item: Vasoview Hemopro Endoscopic Vessel Harvesting System Maquet Cardiovascular...

The Issue: Maquet has received an increase in the number of complaints for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2013· Orthofix, Inc

Recalled Item: Azure Anterior Cervical Plate System Recalled by Orthofix, Inc Due to There...

The Issue: There is a possibility that the locking mechanism of the Azure Anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2013· Thermofisher Scientive

Recalled Item: MAS Urinalysis Control Level 1 Recalled by Thermofisher Scientive Due to Via...

The Issue: Via one (1) consumer complaint and in-house testing has confirmed that the...

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

Class III — Low RiskOngoing
Medical DeviceOctober 28, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam line of gamma camera systems Used to detect or Recalled by Siemens...

The Issue: Reports of loose bolts in the detector support structure of Symbia and e.cam...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Synovis Surgical Innovations, Inc.

Recalled Item: Dura Guard Recalled by Synovis Surgical Innovations, Inc. Due to Synovis, a...

The Issue: Synovis, a subsidiary of Baxter International Inc., is recalling certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Synovis Surgical Innovations, Inc.

Recalled Item: Vascu Guard Recalled by Synovis Surgical Innovations, Inc. Due to Synovis, a...

The Issue: Synovis, a subsidiary of Baxter International Inc., is recalling certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Nephros Inc

Recalled Item: Nephros SafeSpout Manufacturer: Nephros Inc. 41 Grand Avenue Recalled by...

The Issue: Promotional materials for non-medical water filtration products were...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 28, 2013· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: Integra Disposable Recalled by Integra LifeSciences Corp. d.b.a. Integra...

The Issue: Integra LifeSciences Corporation is recalling certain lots of Integra Kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Abbott Point Of Care Inc.

Recalled Item: Abbott i-STAT PT/INR cartridges Abbott Point of Care Inc. Recalled by Abbott...

The Issue: Abbott Point of Care Inc (APOC) has determined that i-Stat PT/INR cartridges...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Toshiba American Medical Systems Inc

Recalled Item: Titan 3T MRI System Recalled by Toshiba American Medical Systems Inc Due to...

The Issue: Toshiba America Medical Systems, Inc. is recalling due to a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia E is a multi-purpose SPECT system ideal for hospitals Recalled by...

The Issue: Reports of loose bolts in the detector support structure of Symbia and E.CAM...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2013· Nephros Inc

Recalled Item: 1) Nephros SafeShower FH - 15 filters per box Recalled by Nephros Inc Due to...

The Issue: Promotional materials for non-medical water filtration products were...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 28, 2013· Nephros Inc

Recalled Item: Nephros Dual Stage Ultra Filter (DSU) Brochure Document 60-3003 Revisions: 0...

The Issue: Promotional materials for non-medical water filtration products were...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 25, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: 1) Accolade II 127 Neck Angle Hip Stem Recalled by Stryker Howmedica...

The Issue: Stryker received a report from the field indicating that an Accolade II Hip...

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

Class II — Potential Health HazardOngoing