Surgify Halo: recall status
⚠ Recalls found. Surgify Halo is named in 19 official recalls in our current data:
- Brand
- SURGIFY MEDICAL OY
Recalls naming this model
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2555-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2556-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2557-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2558-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2559-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2560-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2561-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2562-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2563-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2564-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2565-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2566-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2567-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2568-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2569-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2570-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2571-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2572-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Company / brand: SURGIFY MEDICAL OY recalls
Affected product: Surgify Halo recall status
Official ID Z-2573-2026 ·
Official record ↗
See all SURGIFY MEDICAL OY recalls →
Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.