Class I — AVID Medical, Inc.
| Recalling firm | AVID Medical, Inc. |
|---|---|
| Classification | Class I |
| Status | Ongoing |
| Reason | Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides |
| Product | Halyard IV START KIT NON-STERILE REF: KRIV26-02 |
| Quantity | 288 units |
| Distribution | US Nationwide distribution in the state of NE. |
| Initiated | 2026-07-14 |
| Classified | 2026-09-14 |
| Recall number | Z-3108-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class I recall — AVID Medical, Inc. (Z-3108-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99672/
Alerts for AVID Medical, Inc.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.