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 2298123000 of 27,462 recalls

Medical DeviceJuly 31, 2014· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Mindray V21 Recalled by Mindray DS USA, Inc. dba Mindray North America Due...

The Issue: Mindray DS USA Inc. initiated a voluntary field corrective action for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM Recalled by Wright Medical...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW 3.5mm PLATE CHARLOTTE F&A SYSTEM Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Zimmer, Inc.

Recalled Item: Zimmer Gender Solution Patello-Femoral Joint (PFJ) System Patello-Femoral...

The Issue: Internal review found that five (5) PFJ implant forgings were identified as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2014· Radiometer America Inc

Recalled Item: RADIANCE v. 2.4X Recalled by Radiometer America Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: The Symbia T Series consists of the T16 Recalled by Siemens Medical...

The Issue: Siemens Medical Solutions USA, Inc. is performing a field correction because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2014· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Minstrel (with scale) Product Usage: is a mobile passive hoist. Recalled by...

The Issue: ArjoHuntleigh received three reports where the bolt under the scale...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2014· Illumina Inc

Recalled Item: Illumina Worklist Manager (IWM) (software v1.0.15) Recalled by Illumina Inc...

The Issue: A software component of the MiSeqDx instrument, called the Illumina Worklist...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2014· Becton Dickinson & Co.

Recalled Item: BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen...

The Issue: These lots of Agar may have exhibited breakthrough growth of vancomycin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: The Symbia Intevo series consists of the Intevo 16 Recalled by Siemens...

The Issue: Siemens Medical Solutions USA, Inc. is performing a field correction because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2014· Philips Medical Systems (Cleveland) Inc

Recalled Item: IntelliSpace Portal (ISP) DX/HX/EX Recalled by Philips Medical Systems...

The Issue: The following software issues have been identified in the affected products....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· Galt Medical Corporation

Recalled Item: GALT VALVED TEARAWAY INTRODUCER SET GALT VTI RX ONLY UNITS Recalled by Galt...

The Issue: The adhesive used in the product could dislodge when objects are inserted...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· OrthoPediatrics Corp

Recalled Item: ACL Sleeve Installation Tool Sizes: 6mm Recalled by OrthoPediatrics Corp Due...

The Issue: Weld fractures on the Sleeve Installation Tool for ACL reconstruction system.

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

Class II — Potential Health HazardOngoing