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 2100121020 of 27,462 recalls

Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Pediatric Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Adult Pak P/N: 73124...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (400) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (250) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2015· Integra LifeSciences Corp.

Recalled Item: Universal Compact Head Ring Adapter Plate (UCHRAP) Recalled by Integra...

The Issue: Integra identified that the UCHRAP component (Arc Adapter Plate) would not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2015· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180 Recalled by Olympus...

The Issue: Insufficient information for specific cleaning accessories used for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2015· DJO, LLC

Recalled Item: Monode Recalled by DJO, LLC Due to Overheating and burning of the wire...

The Issue: Overheating and burning of the wire insulation inside the applicator.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2015· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Aliquot Delivery Kit (Syringe and Plunger) Recalled by Orthovita, Inc., dBA...

The Issue: Two isolated instances of holes in the outer header bag component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2015· Covidien LLC

Recalled Item: MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item...

The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2015· Covidien LLC

Recalled Item: Physio-Control QuikCombo Pacing/Defibrillation/ECG Electrodes RediPak¿...

The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound System with software versions VB10B and lower...

The Issue: The ACUSON SC2000 ultrasound system considers uppercase/lowercase...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2015· Covidien LLC

Recalled Item: MediTrace Cadence Adult Zoll Recalled by Covidien LLC Due to Multi-Function...

The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2015· Brainlab AG

Recalled Item: Disposable Marker Spheres The Disposable Marker Spheres used Recalled by...

The Issue: Disposable Marker Spheres (DRMS) for Brainlab Image Guided Surgery (IGS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2015· Medtronic Perfusion Systems

Recalled Item: MEDTRONIC PERFUSION TUBING PACKS (with potentially affected...

The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2015· Medtronic Perfusion Systems

Recalled Item: MEDIVATORS HEMOCOR HPH700 Recalled by Medtronic Perfusion Systems Due to...

The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2015· Apatech Limited

Recalled Item: Actifuse ABX/Actifuse MIS System A bone void filler intended only Recalled...

The Issue: Baxter Healthcare is issuing a voluntary recall for all lots of Actifuse ABX...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software and firmware bugs

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

Class II — Potential Health HazardOngoing