Endo-Model Replacement Plateau Recall
The Endo-Model Replacement Plateau implant (Item Number 15-0027/11) is being recalled because the bushing on the plateau screw can detach from the shaft due to …
Waldemar Link GmbH & Co. KG (Mfg Site)
Every recall we are tracking for Waldemar Link GmbH & Co. KG (Mfg Site), newest first, sourced from the FDA. If you are wondering whether your Waldemar Link GmbH & Co. KG (Mfg Site) 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 Waldemar Link GmbH & Co. KG (Mfg Site) recall posts.
1 recall · updated Jan 12, 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.
Be the first to know if Waldemar Link GmbH & Co. KG (Mfg Site) issues a recall.
Free forever. Unsubscribe anytime. We never sell your data.