Class IIOngoingZ-2556-2026
SURGIFY MEDICAL OY recalls Surgify Halo
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
SURGIFY MEDICAL OYJul 1, 2026
Ongoing recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 133–144 of 4,530 recalls
Class IIOngoingZ-2555-2026
SURGIFY MEDICAL OY recalls Surgify Halo
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
SURGIFY MEDICAL OYJul 1, 2026
Class IIOngoingZ-2554-2026
IPG Medical Corporation recalls Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.
Software anomaly that causes a false display of error code 5018.
IPG Medical Corporatio…MAJul 1, 2026
Class IIOngoingZ-2553-2026
GE Medical Systems SCS recalls GE Healthcare AW Server 3.2 ext.6.5
GE HealthCare has become aware of a context synchronization issue in AW Server 3.2 ext. 6.5. When a user selects a patient or exam in the AW Server Web Client worklist and launches an interactive application (e.g.…
GE Medical Systems SCSJul 1, 2026
Class IIOngoingZ-2552-2026
Stryker Neurovascular recalls INZONE DETACHMENT SYSTEM
Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and visual indicators;…
Stryker NeurovascularCAJul 1, 2026
Class IIOngoingZ-2532-2026
Acumed LLC recalls Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe…
Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use.
Acumed LLCORJul 1, 2026
Class IIOngoingZ-2531-2026
Zimmer, Inc. recalls Off-Axis Alliance Glenoid
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Zimmer, Inc.INJul 1, 2026
Class IIOngoingZ-2530-2026
Zimmer, Inc. recalls Off-Axis Alliance Glenoid
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Zimmer, Inc.INJul 1, 2026
Class IIOngoingZ-2529-2026
Zimmer, Inc. recalls Off-Axis Comprehensive Shoulder System
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Zimmer, Inc.INJul 1, 2026
Class IIOngoingZ-2528-2026
Zimmer, Inc. recalls Off-Axis Comprehensive Shoulder System
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Zimmer, Inc.INJul 1, 2026
Class IIOngoingZ-2527-2026
Zimmer, Inc. recalls Off-Axis Comprehensive Shoulder System Small
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Zimmer, Inc.INJul 1, 2026
Class IIOngoingZ-2526-2026
PFM MEDICAL INC. recalls Multi-Snare Set: 5 mm x 125 cm
A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility requirements for in-vitro-cytotoxicity, which if in contact with a…
PFM MEDICAL INC.CAJul 1, 2026