MicroVention LVIS Stent Device Recall
MicroVention's LVIS Intraluminal Support Device (stent) may have incorrect dimensions or configuration due to a manufacturing issue. If the stent is the wrong …
MICROVENTION INC.
MICROVENTION INC. Recalls (2026)
Every recall we are tracking for MICROVENTION INC., newest first, sourced from the FDA. If you are wondering whether your MICROVENTION INC. 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 MICROVENTION INC. recall posts.
1 recall · updated Apr 6, 2026
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SUNS International SS6291 Elevator Switch Recall
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 StrikeLock Door Lock Recall
Residential Elevators is recalling its StrikeLock hoistway door locking device, used on residential elevator landing doors. The defective lock can allow the …
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BD PurPrep Povidone-Iodine Recall
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 …
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BD PurPrep Povidone-Iodine Recall
BD PurPrep povidone-iodine sterile solution applicators (10.5 mL, 25-pack) are being recalled because the manufacturer cannot confirm they are properly …
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Philips SmartPath dStream MRE Recall
Philips SmartPath to dStream 3.0T MR Elastography systems can produce incorrect stiffness measurements when certain image settings are used together. This may …
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Physio-Control LIFEPAK Defibrillator Recall 2026
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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