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. 2,856 recalls have been distributed to Texas in the last 12 months.
Showing 10501–10520 of 55,713 recalls
Recalled Item: VITROS XT 7600 Integrated System - For use in the in vitro quantitative...
The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System - . For use in Recalled by Ortho-Clinical...
The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Storage and Retrieval Module (SRM)-Laboratory Automation system Brand names...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Input Output Module (IOM) FLX-201-Laboratory Automation system Brand names...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vesmatic Cube 80 Interface Module (VMC)-Laboratory Automation system Brand...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PVT Interface Module (PVT)-Laboratory Automation system Brand names of the...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity h Interface Module (HSQ)-Laboratory Automation system Brand names of...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Pak Surgical Procedure Pack: Pak Number & Pak Recalled by Alcon...
The Issue: Sterility; Steril surgical procedure packs contain incomplete seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JARDIANCE (Empagliflozin) Recalled by Boehringer Ingelheim Pharmaceuticals,...
The Issue: Labeling: Label Mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dofetilide Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DEVILBISS HEALTHCARE 1025 SERIES OXYGEN CONCENTRATOR Recalled by DeVilbiss...
The Issue: The instruction manual is being replaced with an updated version that is in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti-SARSCoV- 2 Total N Antibody...
The Issue: Incorrect Number of Calibrator Levels (2) Set for the VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost C50 -intended for use in generating radiographic...
The Issue: If the PM for the telescopic carriage is not performed annually as defined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C50 1.1-intended for use in generating radiographic images...
The Issue: If the PM for the telescopic carriage is not performed annually as defined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEKTOVI (binimetinib) tablets Recalled by Pfizer Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: The carton and bottle...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MectaLIF ANTERIOR - Lag Plate Flush H10 Recalled by Medacta Usa Inc Due to...
The Issue: There is a potential for breakage of the small screw used to affix the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQURE Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 Recalled by Radiometer...
The Issue: Due to potential software issue that may result in patient mix-up information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MectaLIF ANTERIOR - Lag Plate Flush H14 Recalled by Medacta Usa Inc Due to...
The Issue: There is a potential for breakage of the small screw used to affix the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Gastrointestinal (GI) Panel for FILMARRAY Systems Recalled by...
The Issue: Due to manufacturing issue, Gastrointestinal (GI) Panel may result in false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MectaLIF ANTERIOR - Antibackout Lag Cover Recalled by Medacta Usa Inc Due to...
The Issue: There is a potential for breakage of the small screw used to affix the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.