Product Recalls in West Virginia

Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,473 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,473 in last 12 months

Showing 1542115440 of 27,884 recalls

Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT Recalled by Integra LifeSciences...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer (SMN 11067000) . The Atellica" Solution Recalled by...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer (SMN 11066001). The Atellica" Solution is Recalled...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Connect (SMN 11069018). The Atellica" Solution is...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Additional (SMN 11069004). The Atellica" Solution is...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer (SMN 11066000). The Atellica" Solution is Recalled...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Prime (SMN 11069001). The Atellica" Solution is...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Quasar Bio-Tech, Inc.

Recalled Item: Baby Quasar Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...

The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Quasar Bio-Tech, Inc.

Recalled Item: Quasar MD Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...

The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Luminex Corporation

Recalled Item: Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 Recalled by...

The Issue: An incorrect control board and firmware installed in some of the Hand Held...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: 3D TOP Ceiling Stand Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: In rare cases of insufficient maintenance or high clinical workload, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD Infinity XR2 Base Unit-Extended Recalled by Integra LifeSciences...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD INFINITY XR2 BASE UNIT Recalled by Integra LifeSciences Corp. Due...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Integra LifeSciences Corp.

Recalled Item: MAYFIELD SPINE TABLE ADAPTOR RADIOLUCENT Recalled by Integra LifeSciences...

The Issue: There is a potential for the knob assembly in the swivel adapter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation stand-alone software treatment planning system Recalled by...

The Issue: If the beam model has a highly asymmetric primary source, it is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250/MEVION S250i Proton Beam Radiation therapy system Product Usage:...

The Issue: QFix has advised Mevion Medical Systems that they are identifying...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: 3D V Recalled by Siemens Medical Solutions USA, Inc Due to In rare cases of...

The Issue: In rare cases of insufficient maintenance or high clinical workload, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Quasar Bio-Tech, Inc.

Recalled Item: Pure Rayz Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not receive...

The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2018· Bayer Medical Care, Inc.

Recalled Item: Overhead Counterpoise Systems (OCS) OCS CONF an accessory device for...

The Issue: The torque wrench used on the ceiling column assembly during a recent...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2018· Bayer Medical Care, Inc.

Recalled Item: Overhead Counterpoise Systems (OCS) Recalled by Bayer Medical Care, Inc. Due...

The Issue: The torque wrench used on the ceiling column assembly during a recent...

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

Class II — Potential Health HazardOngoing