Broviac 4.2 Fr Catheter Cutdown Tray Recall
Bard Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff (Cat 60060) is being recalled due to potential damage to the outer …
Bard Peripheral Vascular Inc
Every recall we are tracking for Bard Peripheral Vascular Inc, newest first, sourced from the FDA. If you are wondering whether your Bard Peripheral Vascular 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 Bard Peripheral Vascular Inc recall posts.
1 recall · updated Dec 12, 2025

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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