Class IIOngoingZ-2561-2026
SURGIFY MEDICAL OY recalls Surgify Halo
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
SURGIFY MEDICAL OYJul 1, 2026
Drills, Burrs, Trephines & Accessories (Simple, Powered) recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 13–24 of 24 recalls
Class IIOngoingZ-2560-2026
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-2559-2026
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-2558-2026
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-2557-2026
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-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
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-2461-2025
Medtronic Xomed, Inc. recalls IPC Powerease System REF 2300000 UDI-DI: 00613994448705 00643169406834. The IPC P…
Due to out of the box wobble of the driver.
Medtronic Xomed, Inc.FLSep 3, 2025
Class IIOngoingZ-2192-2025
Phasor Health, LLC recalls Phasor Drill
Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.
Phasor Health, LLCTXAug 6, 2025
Class IIOngoingZ-0982-2025
Stryker Corporation recalls stryker 3.0MM Precision Neuro Match Head
There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).
Stryker CorporationMIJan 29, 2025
Class IIOngoingZ-0981-2025
Stryker Corporation recalls stryker 3.0MM Neuro Match Head
There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).
Stryker CorporationMIJan 29, 2025
Class IIOngoingZ-0980-2025
Stryker Corporation recalls The 3.0MM Neuro Match Head Soft Touch bur (5820-107-030) is intended to be used to cut…
There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-030 but package contains a 5820-107-530 device).
Stryker CorporationMIJan 29, 2025