Class I — AVID Medical, Inc.
| Recalling firm | AVID Medical, Inc. |
|---|---|
| Classification | Class I |
| Status | Ongoing |
| Reason | Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides. |
| Product | Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02. |
| Quantity | 288 kits (6 cases) |
| Distribution | US Nationwide distribution. |
| Initiated | 2026-07-22 |
| Classified | 2026-09-23 |
| Recall number | Z-3194-2026 |
| 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-3194-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99761/
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