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. 2,697 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,697 in last 12 months

Showing 2312123140 of 55,713 recalls

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· 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· 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· 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
DrugJuly 8, 2019· Piramal Critical Care, Inc.

Recalled Item: Gablofen (baclofen injection) Recalled by Piramal Critical Care, Inc. Due to...

The Issue: Failed Impurities/Degradation Specification -This recall is being initiated...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 8, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACS Sample Prep Assistant (SPA) II Upgrade - Product Recalled by Becton,...

The Issue: The recalling firm confirmed that SPA II and III users may encounter probes...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACS Sample Prep Assistant (SPA) II - Product Usage: Recalled by Becton,...

The Issue: The recalling firm confirmed that BD FACS Sample Prep Assistant (SPA) II and...

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

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

Recalled Item: Visualase Cooled Laser Applicator System Tubing Set kits Product numbers:...

The Issue: The firm received complaints on the saline tubing of Visualase Cooled Laser...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACS Sample Prep Assistant (SPA) III - Product Usage: Recalled by Becton,...

The Issue: The recalling firm confirmed that SPA II and III users may encounter probes...

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· 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· 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· Xcision Medical Systems, LLC

Recalled Item: GammaPod Stereotactic Radiotherapy System Model A Recalled by Xcision...

The Issue: One bolt on the V motor was not fully tightened which caused a drift of .13...

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 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· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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
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· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Drive Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing