INZONE DETACHMENT SYSTEM: recall status

⚠ Recall found. INZONE DETACHMENT SYSTEM is named in 1 official recall in our current data. Details and the official notices are below — act on the remedy in the official notice.

Brand: Stryker Neurovascular

Recalls naming this model

FDA Class II · Medical device · July 1, 2026

INZONE DETACHMENT SYSTEM recall — Stryker Neurovascular

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; 3) Be …

Official ID Z-2552-2026 · Official record ↗

See all Stryker Neurovascular 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.