Covidien Mon-a-Therm Temperature Probe Recall
Covidien Mon-a-Therm temperature probe (9 Fr, REF 90050) was sold without FDA clearance. The company initiated a voluntary withdrawal because these devices lack …
Covidien LLC
Covidien LLC Recalls (2026)
Every recall we are tracking for Covidien LLC, newest first, sourced from the FDA. If you are wondering whether your Covidien 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 Covidien LLC recall posts.
1 recall · updated Apr 23, 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
Draeger Atlan A350XL Anesthesia Workstation Recall
Draeger has recalled the Atlan A350XL anesthesia workstation (model 8621600) because the device may signal a piston ventilator failure before use, or the …
Draeger, Inc.
B. Braun Spinocan Spinal Needle Kit Recall
B. Braun Medical is recalling three Spinocan spinal needle procedure kits that contain Bupivacaine 0.75% with Dextrose 8.25% injection. The bupivacaine inside …
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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 …
Residential Elevators StrikeLock Hoistway Door Locking Device
BD Spinal Tray Whitacre Needle 405645 Recall
Becton Dickinson is recalling a spinal anesthesia tray because one of its drug components, bupivacaine hydrochloride in dextrose injection, was made at a …
Becton Dickinson & Company
Covidien Mon-a-Therm Temperature Probe Recall
Covidien Mon-a-Therm temperature probe (9 Fr, REF 90050) was sold without FDA clearance. The company initiated a voluntary withdrawal because these devices lack …
Covidien LLC
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