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. 2,790 recalls have been distributed to Texas in the last 12 months.
Showing 15681–15700 of 55,713 recalls
Recalled Item: Foundation Kit Recalled by Stradis Medical, LLC dba Stradis Healthcare Due...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls...
The Issue: VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab (FLX) Recalled by Inpeco S.A. Due to The Firmware (FW) of the...
The Issue: The Firmware (FW) of the Automation System Interface Module to ADVIA Centaur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evita V500 Ventilator with Installed CO2 Measurement Option-Intended for the...
The Issue: Software 2.51 and Lower with Installed CO2 Measurement Option, may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tenaculum Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rocuronium Bromide Injection 50mg/5 mL Recalled by Piramal Critical Care,...
The Issue: Labeling: Label Lacks Warning or Rx Legend: Finished product did not include...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kroger 70% Isopropyl Alcohol First Aid Antiseptic 32 FL OZ Recalled by...
The Issue: Labeling: Label Mix-Up.The recall has been initiated after receiving one...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Tartrate Tablets USP 100 mg Recalled by Aurobindo Pharma USA Inc....
The Issue: Presence of Foreign Substance: Product complaints received for the presence...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TomoHelical and TomoDirect plans in RayStation 6 Recalled by RAYSEARCH...
The Issue: If the dynamic jaw mode is used and an optimization is continued after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee Recalled by...
The Issue: Packaging may include screws that are not intended to be used with the 5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may unexpectedly shut down when the device is running on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vit Kit-Freeze is intended for use in assisted reproductive procedures...
The Issue: Due to a component in kit being labeled with the incorrect Expiration Date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Helium Indicator on the Cardiosave display may over represent the amount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Helium Indicator on the Cardiosave display may over represent the amount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may unexpectedly shut down when the device is running on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Nexiva Recalled by Becton Dickinson Infusion Therapy Systems Inc. Due to...
The Issue: There is a breach in the product packaging that renders the product non-sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vit Kit-Freeze is intended for use in assisted reproductive procedures...
The Issue: Due to a component in kit being labeled with the incorrect Expiration Date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chesapeake Anterior Lumbar (AL) Removal Tool Recalled by K2M, Inc Due to...
The Issue: Units may arrive with missing pins and/or in a state in disassembly. Pins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraTears Extra (sodium carboxymethylcellulose) 0.25% Lubricant Eye Drops...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GEL CONDUCTOR Recalled by DJO, LLC Due to Ultrasound gels and lotions...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.