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All product recalls affecting Pennsylvania.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Pennsylvania in the distribution area.
Production assembly error resulting in the potential for reversed articulation, where moving the lever forward caused the probe tip to anteflex rather than retroflex, and vice versa.
Fontaine Trailer Company (Fontaine Trailer) is recalling certain 2025-2026 Fontaine HCIFL12SAT and HCIFL82CTA forklift trailers. The auto lift axle cables may not be installed in the correct ports, which can disable the anti-lock brake system. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 121, "Air Brake Systems."
REV Recreation Group (REV) is recalling certain 2023-2024 American Coach American Tradition, 2023-2026 American Eagle, and American Dream, and 2025-2026 Fleetwood Palisade recreational vehicles. The waste tank macerator fuse may overheat, causing the fuse housing to melt.
Tuff Trailer USA Inc. (Tuff Trailer) is recalling certain 2024 USA TTA17200T and USA TTA18200T trailers. The Gross Vehicle Weight Rating (GVWR) listed on the coupler label may be incorrect.
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
To provide further information to the user to ensure proper use of the medical device. the caps had been changed from a threaded version to a press-on version whereby the user must press the caps firmly onto the dialyzer to securely affix the cap.
IV sets may leak.
IV sets may leak.
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Kibbi, LLC (Kibbi) is recalling certain 2024-2025 Renegade Verona and Verona LE recreational vehicles. The rear leveling jack mounting bracket may contact and deflate the rear suspension air bag, lowering the rear suspension.
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
IV sets may leak.
IV sets may leak.
IV sets may leak.
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Potential for device to overheat during operation f the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure alarm is not triggered.
IV sets may leak.
Lack of Assurance of Sterility
Hiab USA Inc. (Hiab) is recalling certain Galfab NIO 75 194 SO 72R, NOR 75 194 SO 72R, and OR 75 194 SO 72R reverse hoists. The upper hoist cylinder mounting pin may fail.
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.