Reported Oct 28, 2026 · Ongoing · Updated Nov 2, 2026

Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH30.

AVID Medical, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: AVID Medical, Inc. · 9000 Westmont Dr · Toano, VA · 23168-9351

Is this the product you have?

  • Halyard ANTERIOR HIP PACK
  • Model/Catalog NumberSOAH30
Lot codes and dates
  • Model/Catalog NumberSOAH30
  • UDI-DI10809160520246
  • Lot CodeLot
  • Numbers
    • 1705826
    • 1705827
  • Expiration Date1/31/2028
Amount recalled
80 kits

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide
  • AZ

Why it was recalled

A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Nov 4, 12:15 AM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.