Surgify Halo Surgical Burr Recall
Surgify Halo 5.4 mm Medium burr drills (Model 54.085.SHD.H1) used in spinal surgery can break during the procedure. A broken burr could complicate surgery or …
SURGIFY MEDICAL OY
Every recall we are tracking for SURGIFY MEDICAL OY, newest first, sourced from the FDA. If you are wondering whether your SURGIFY MEDICAL OY 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 SURGIFY MEDICAL OY recall posts.
1 recall · updated Apr 30, 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
The Medtronic O-arm O2 Imaging System (Model BI70002000) can produce distorted or incorrect images due to a firmware defect in its detector panel. This imaging …
Medtronic Navigation, Inc.-Boxborough
Inspire Stimulation Lead (Model 4063) devices are labeled with incorrect expiration dates that extend beyond their validated three-year shelf life. Using an …
Inspire Medical Systems Inc.
Fresenius Bicarby Dialysate (Model RFP-400-G) has an incorrect barcode label that could lead to the wrong potassium concentration being used during dialysis. …
Fresenius Medical Care Holdings, Inc.
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 Medical is recalling three Spinocan spinal needle procedure kits that contain Bupivacaine 0.75% with Dextrose 8.25% injection. The bupivacaine inside …
B Braun Medical Inc
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