Drug recall
Halyard IV Start Kit Non-Sterile REF: KRIV26-02
FDA recall event 99525 · Class II · AVID Medical, Inc.
Key facts
| Event ID | 99525 |
|---|---|
| Recall numbers | Z-3109-2026 |
| Recalling firm | AVID Medical, Inc. |
| Product type | Devices |
| Products | Halyard IV Start Kit Non-Sterile REF: KRIV26-02 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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. |
| Initiation date | Jul 14, 2026 |
| Report date | Sep 16, 2026 |
| City | Toano |
| State | VA |
| Country | United States |
| FEI number | 1047429 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: