FDA Class II · Medical device · August 26, 2026
GETINGE Y SENSOR Module recall — Maquet Critical Care AB
The module did not undergo electrical safety tests and functional tests during production.
Official ID Z-2963-2026 · Official record ↗
Maquet Critical Care AB recalls
2 recent recalls on record for Maquet Critical Care AB in connected official government data as of October 22, 2026 at 6:00 PM UTC.
Models with recalls
Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C2 (1)GETINGE Y SENSOR Module (1)
All Maquet Critical Care AB recalls
FDA Class II · Medical device · August 12, 2026
Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C2 recall — Maquet Critical Care AB
Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient receiving insufficient …
Official ID Z-2860-2026 · Official record ↗
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 & processed egg products ↗ (not 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 government data. Last checked October 22, 2026 at 6:00 PM UTC.