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All product recalls affecting Texas.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Texas in the distribution area.
contaminated with Bacillus cereus and may be spoiled
REV Recreation Group (REV) is recalling certain 2025-2026 Holiday Rambler Incline, and Fleetwood Altitude Class C motorhomes. The electrical components under the house entry steps may fail due to water intrusion, including the carbon monoxide (CO) or Liquid Propane (LP) detector.
Evenflo Company, Inc. (Evenflo) is recalling certain Titan 65 child seats with model number 3712198 manufactured between March 17, 2025 and May 1, 2025. The child seat may have been packaged with an incorrect instruction manual. As such, these child seats and travel systems fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 213, "Child Restraint Systems."
Tesla, Inc. (Tesla) is recalling certain 2026 Model 3 and Model Y vehicles. The fasteners attaching the seat back to the seat bottom may have been improperly tightened.
Due to an incorrect test results provided that indicated the incorrect drug therapy recommendation
Potential for faulty devices as a result of depleted batteries.
Dipstick strep A test has potential for false positive results.
A software update for Medtronic CareLink SmartSync Device Manager (SmartSync) is now available. The update eliminates the potential display of an erroneous electrical reset (pop-up) message upon interrogation with a SmartSync Device Manager. The erroneous message indicates an electrical reset has occurred. However, no reset has actually occurred and there are no parameter changes or loss of diagnostics. Prior to this software update, if an erroneous SmartSync message was displayed, confusion regarding the message could have caused a clinician to consider an unnecessary system revision. Medtronic has received 39 reports of this display error with two instances of unnecessary device explant through 30 April 2025.
Review of Label determined allergen was listed as unsalted butter/ heavy cream. In one instance of identified label, there was no milk or dairy listed listed in Contains statement. Further review of label revealed "soy" had been removed.
SwabFlush syringes are affected by the ICU Medical recall of their SwabCap Disinfecting Cap due to a manufacturing issue which affects the seal between the foil lid and plastic container of the Swab Cap. The issue may result in a reduced level of disinfection of the luer access valve, potentially resulting in patient infection/sepsis.
Lens blisters may have an incomplete or leaking seal which may render them unsterile.
Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
Closed system drug transfer devices were shipped to the U.S. market without a U.S. version of the instructions for use, which could be an issue if a healthcare professional is prompted to review it.
Lens blisters may have an incomplete or leaking seal which may render them unsterile.
Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
Labeling: Incorrect or Missing Lot and/or Exp. Date: A printing issue resulted in incorrect lot numbers on the label.
Lack of assurance of sterility: pinholes, within the finger boxes used during Form Fill Seal process resulting in leaks.
Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 9 month long term stability station (25¿C, 60%RH).
Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.