# Class II recall Z-0283-2027: AVID Medical, Inc.

**Predicate Speed & CAPA Advisory Opportunity Score:** 68/100

| Field | Value |
|---|---|
| Record | Device recall |
| Recall number | Z-0283-2027 |
| Recalling firm | AVID Medical, Inc. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary / mandated | Voluntary: Firm initiated |
| Specialty | Other |
| Product | Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH30. |
| Reason | A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications. |
| Quantity | 80 kits |
| Distribution | US Nationwide distributor in the state of Arizona. |
| Recall initiated | 2026-09-08 |
| Reported | 2026-10-28 |
| Firm location | Toano, VA, United States |

## Why this score
- Class II recall: usually triggers CAPA and quality-system remediation work.
- Recall is still ongoing.
- Posted 8 days ago.

Source: U.S. FDA openFDA (510(k) clearances and device enforcement reports) (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0283-2027%22). Last refreshed: 2026-11-04T09:16:12.111Z.
Data from the FDA openFDA API, which may lag official FDA databases. Informational only; not regulatory or legal advice.