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All product recalls affecting Pennsylvania.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Pennsylvania in the distribution area.
This recall involves all VINs of Polaris Model Year 2023-2024 Ranger XP Kinetic and Model Year 2025 Pro XD Kinetic ROVs. The recalled Ranger XP Kinetic vehicles were sold in camouflage and white colors. The recalled Pro XD vehicles have gray plastic body panels with a black frame and accents. All vehicles were sold in three-seat configurations and have "POLARIS" stamped on the front grille. The VIN is printed on a portion of the left rear frame (on the driver's side of the vehicle) under the cargo box. In addition, this recall involves accessory charger service parts/kits with part numbers 2417296, 2417297, 2889704 and 2889486.
Clostridium botulinum (uneviscerated fish)
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.
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.
undeclared milk allergen
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.