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. 2,510 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,510 in last 12 months

Showing 1308113100 of 27,462 recalls

Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho Clinical Diagnostics Due to Potential...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 250 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 250 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho Clinical Diagnostics Due to Potential...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 32 Recalled by Ortho Clinical...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 250AT Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 350 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 32 Recalled by Ortho Clinical...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Capso Vision, Inc.

Recalled Item: CapsoCam Plus *** System Recalled by Capso Vision, Inc. Due to Possible...

The Issue: Possible mis-labeling of the device with incorrect serial number labels...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· LivaNova USA Inc.

Recalled Item: LivaNova SMART PERFUSION PACK INSPIRE 8S - Product Usage: The Recalled by...

The Issue: Perfusion tubing pack was packaged with the incorrect cuvette.

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 20 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 30 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 40 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 20 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 30 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Heidelberg Engineering GmbH

Recalled Item: SPECTRALIS with HEYEX2 image management system. a non-contact ophthalmic...

The Issue: Error in the default configuration which could lead to the incorrect display...

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

Class II — Potential Health HazardOngoing