Arjo Tenor Patient Lift Recall
Certain Arjo Tenor mobile patient lifts may have a defective internal component in the actuator that could suddenly lose its ability to hold the load, causing …
ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Every recall we are tracking for ARJOHUNTLEIGH POLSKA Sp. z.o.o., newest first, sourced from the FDA. If you are wondering whether your ARJOHUNTLEIGH POLSKA Sp. z.o.o. product is recalled in 2026, check the list below for your model, lot, or VIN. Each entry explains the hazard and the free repair, replacement, or refund. Get a free email alert the moment a new ARJOHUNTLEIGH POLSKA Sp. z.o.o. recall posts.
1 recall · updated Mar 10, 2026

SUNS International is recalling SS6291 Solenoid Interlock Switches used in residential elevators because the switch can get stuck in a retracted position, …
SUNS SS6291 Solenoid Interlock Switches

Residential Elevators is recalling its StrikeLock hoistway door locking device, used on residential elevator landing doors. The defective lock can allow the …
Residential Elevators StrikeLock Hoistway Door Locking Device
BD PurPrep povidone-iodine sterile skin prep solution (25 applicators per carton) may not be sterile due to potential product contamination. Using a non-sterile …
CareFusion 213, LLC
BD PurPrep povidone-iodine sterile solution applicators (10.5 mL, 25-pack) are being recalled because the manufacturer cannot confirm they are properly …
CareFusion 213, LLC
Philips SmartPath to dStream 3.0T MR Elastography systems can produce incorrect stiffness measurements when certain image settings are used together. This may …
Philips North America
Physio-Control is recalling certain LIFEPAK defibrillators that were serviced between July 2023 and November 2025 without confirmed completion of a required …
Physio-Control, Inc.
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