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. 2,526 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,526 in last 12 months

Showing 1146111480 of 27,462 recalls

Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8B Recalled by RAYSEARCH LABORATORIES AB Due to Software error...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 9B Service Pack 1 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8A Recalled by RAYSEARCH LABORATORIES AB Due to Software error...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 7 Recalled by RAYSEARCH LABORATORIES AB Due to Software error was...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8B Service Pack 2 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 4.0 to RayStation 5 Service Pack 2 - Product Recalled by...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 6 Recalled by RAYSEARCH LABORATORIES AB Due to Software error was...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 9B Recalled by RAYSEARCH LABORATORIES AB Due to Software error...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 6 Service Pack 1 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8B Service Pack 1 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: 3COR DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due to...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: 3COR DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due to...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Mediana Co., Ltd.

Recalled Item: DIRECT SUPPLY Attendant VITAL SIGNS MONITOR Recalled by Mediana Co., Ltd....

The Issue: Failures were found in the temperature measurement function while in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: (1) CentraLink Data Management System software version 16.0.2 Siemens...

The Issue: Unexpected interface driver behavior identified (QC) Results May Be Assigned...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics Inc.

Recalled Item: Siemens IMMULITE 2000 Immunoassay System - In vitro Chemistry Analyzer...

The Issue: Flexible tubing connected to the liquid waste bottle can crack during...

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

Class II — Potential Health HazardOngoing