FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2555-2026 · Official record ↗
Surgify Halo: recall status
⚠ Recall found. Surgify Halo is named in 19 official recalls in our current data. Details and the official notices are below — act on the remedy in the official notice.
Recalls naming this model
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2556-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2557-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2558-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2559-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2560-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2561-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2562-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2563-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2564-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2565-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2566-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2567-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2568-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2569-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2570-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2571-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2572-2026 · Official record ↗
FDA Class II · Medical device · July 1, 2026
Surgify Halo recall — SURGIFY MEDICAL OY
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Official ID Z-2573-2026 · Official record ↗
See all SURGIFY MEDICAL OY recalls →
Verify with the official sources:
- CPSC — consumer products ↗ (aggregated here)
- NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
- FDA — food, drugs, medical devices ↗ (aggregated here)
- USDA FSIS — meat, poultry & egg products ↗ (not yet aggregated here)
- Recalls.gov — the U.S. government’s all-agency portal ↗
Found something wrong or missing? Report a data error.
Compiled from official public-domain CPSC, NHTSA, and FDA data. Sources last checked July 24, 2026 at 1:09 AM UTC.