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 1832118340 of 27,462 recalls

Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(64)-3R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT X-3R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT 20 Excel Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT Flow 40-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(40)-3R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT Flow Edge-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Medtronic Navigation, Inc.

Recalled Item: AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed Recalled by...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the AxIEM...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Great Basin Scientific, Inc.

Recalled Item: Great Basin Staph lD/R Blood Culture Panel The Great Basin Recalled by Great...

The Issue: The Great Basin Staph ID/R Panel is being recalled because the S. aureus...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· MEDLINE IND

Recalled Item: Medline E-Z Lubricating Jelly Recalled by MEDLINE IND Due to Product was not...

The Issue: Product was not sterilized. Product was shipped to distribution centers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Olympus Corporation of the Americas

Recalled Item: Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The...

The Issue: Olympus has received complaints regarding the breakage of the endoscope's...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Olympus Corporation of the Americas

Recalled Item: URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope Recalled...

The Issue: Olympus is recalling the URF-P6/P6R endoscopes due to a similar device...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Pentax of America Inc

Recalled Item: Rigid Laryngostroboscopes The Rigid Laryngostroboscopes Recalled by Pentax...

The Issue: Pentax is initiating a Field Correction to revise the Instructions for Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System Recalled...

The Issue: Merge received reports of Merge Eye Station being unable to capture images...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2016· Bard Access Systems

Recalled Item: StatLock¿ PICC Plus Crescent Foam. Product Code: VPPCSP & VPPCSPCE. Recalled...

The Issue: Bard Access Systems announces a voluntary field action for the StatLock¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2016· Bard Access Systems

Recalled Item: StatLock¿ CV Plus w/Pigtail. Product Code: CV0220CE & CV0220. Packaged...

The Issue: Bard Access Systems announces a voluntary field action for the StatLock¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q/Q.zen Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens initiated a corrective action to address two possible, mutually...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2016· Trilliant Surgical Ltd.

Recalled Item: Tiger Screw Sterilization Tray Base Assembly Model 210-00-001 Revision N...

The Issue: Four lots of Tiger Screw Sterilization Tray Base Assemblies were released to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products UPRO Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: There is a potential for variable negatively and positively biased urine...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens initiated a corrective action to address two possible, mutually...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Tibial Component Fixed Hinge Small Long Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing