Inspire Stimulation Lead 4063 Recall
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.
Inspire Medical Systems Inc. Recalls (2026)
Every recall we are tracking for Inspire Medical Systems Inc., newest first, sourced from the FDA. If you are wondering whether your Inspire Medical Systems 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 Inspire Medical Systems Inc. recall posts.
1 recall · updated May 11, 2026
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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
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 …
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Inspire Stimulation Lead 4063 Recall
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 RFP-400-G Recall
Fresenius Bicarby Dialysate (Model RFP-400-G) has an incorrect barcode label that could lead to the wrong potassium concentration being used during dialysis. …
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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 …
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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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