Drug recall
Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08
FDA recall event 98060 · Class I · AVID Medical, Inc.
Key facts
| Event ID | 98060 |
|---|---|
| Recall numbers | Z-1000-2026, Z-1001-2026, Z-1002-2026 |
| Recalling firm | AVID Medical, Inc. |
| Product type | Devices |
| Products | Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08, Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17., Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15. |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Devices are not suitable for organ transplant. |
| Initiation date | Nov 11, 2025 |
| Report date | Jan 14, 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: