FDA Class II · Medical device · June 17, 2026
Halyard recall — AVID Medical, Inc.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Official ID Z-2407-2026 · Official record ↗
Halyard: recall status
⚠ Recall found. Halyard is named in 4 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 · June 17, 2026
Halyard recall — AVID Medical, Inc.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Official ID Z-2408-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Halyard recall — AVID Medical, Inc.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Official ID Z-2409-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Halyard recall — AVID Medical, Inc.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Official ID Z-2410-2026 · Official record ↗
See all AVID Medical 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 5:00 AM UTC.