Product Recalls in Texas

Product recalls affecting Texas — including food, drugs, consumer products, medical devices, and vehicles distributed to Texas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,136 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,136 in last 12 months

Showing 14061–14080 of 30,921 recalls

Medical DeviceJuly 10, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 1000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There is a potential for low discordant progesterone results on a subset of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2019· B. Braun Medical, Inc.

Recalled Item: ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT Catalog # 339114 Recalled by B....

The Issue: The filter capacity is not achieved due to damage of the filter membrane.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Phadia Ab

Recalled Item: Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by...

The Issue: code 7-102 Liquid Sensor Error

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915...

The Issue: Potential of an open port in the quench venting system when using the...

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· Smiths Medical ASD Inc.

Recalled Item: GRIPPER Needles sold individually. Labeled as the following item...

The Issue: Potential for certain GRIPPER Needles to contain an occluded or blocked needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Smiths Medical ASD Inc.

Recalled Item: GRIPPER Needles sold as part of PORT-A-CATH II SINGLE LUMEN Recalled by...

The Issue: Potential for certain GRIPPER Needles to contain an occluded or blocked needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· CooperSurgical, Inc.

Recalled Item: TransWarmer Warming Infant Transport Mattress Recalled by CooperSurgical,...

The Issue: The firm updated the IFU in April 2019 to clarify that use of the...

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