Class II — AVID Medical, Inc.
| Recalling firm | AVID Medical, Inc. |
|---|---|
| Classification | Class II |
| Status | Ongoing |
| Reason | Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal area. |
| Product | Halyard IV Start Kit Non-Sterile REF: KRIV26-02 |
| Quantity | 98 Kits |
| Distribution | US Nationwide distribution in the state of NE. |
| Initiated | 2026-07-14 |
| Classified | 2026-09-04 |
| Recall number | Z-3109-2026 |
| 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 II recall — AVID Medical, Inc. (Z-3109-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99525/
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