Gentuity HF-OCT Imaging System Recall
The Gentuity HF-OCT Imaging System Model G10-01 with certain software versions can produce repeated frames during imaging pullbacks, which may lead to …
Gentuity, LLC
Every recall we are tracking for Gentuity, LLC, newest first, sourced from the FDA. If you are wondering whether your Gentuity, LLC 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 Gentuity, LLC recall posts.
1 recall · updated Mar 23, 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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