CGuard Prime Carotid Stent Recall
The CGuard Prime Carotid Stent System (model CND0840) may encounter deployment complications that prevent the stent from being placed properly during the …
INSPIREMD Inc
INSPIREMD Inc Recalls (2026)
Every recall we are tracking for INSPIREMD Inc, newest first, sourced from the FDA. If you are wondering whether your INSPIREMD 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 INSPIREMD Inc recall posts.
1 recall · updated May 1, 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
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. …
Fresenius Medical Care Holdings, Inc.
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 …
B Braun Medical Inc
CGuard Prime Carotid Stent Recall
The CGuard Prime Carotid Stent System (model CND0840) may encounter deployment complications that prevent the stent from being placed properly during the …
INSPIREMD Inc
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
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