Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH31. recall (AVID Medical, Inc.)
Medical deviceClass IIOngoing
Summary: AVID Medical, Inc. is recalling Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH31.. Reason: A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications.
What is being recalled
Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH31.
Why
A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distributor in the state of Arizona. (states named: Arizona)
How to tell if yours is affected
Model/Catalog Number: SOAH31. UDI-DI: 10809160512890. Lot Code: Lot Number: 1689215. Expiration Date: 11/06/2026.
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-0282-2027 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | September 8, 2026 |
| Reported | October 28, 2026 |
| Company | AVID Medical, Inc. |
| Company location | Toano, VA, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 56 kits |
More recalls from AVID Medical, Inc. · all medical device recalls · recalls from September 2026