Medtronic O-arm O2 Imaging System Recall
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
Every recall we are tracking for Medtronic Navigation, Inc.-Boxborough, newest first, sourced from the FDA. If you are wondering whether your Medtronic Navigation, Inc.-Boxborough 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 Medtronic Navigation, Inc.-Boxborough recall posts.
1 recall · updated May 19, 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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