Data Foundry

Medical device recalls 2022

Anterior Hip Pack — Class II medical device recall Z-0865-2022

Ongoing recall by Stradis Medical, LLC dba Stradis Healthcare, reported 2022-04-13, distributed nationwide. The outer bag may be perforated or torn, which may result in a breach in the sterility of the kit.

Recall numberZ-0865-2022
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmStradis Medical, LLC dba Stradis Healthcare, Peachtree Corners, GA, United States
Recall initiated2022-02-25
Classified2022-04-04
Reported by FDA2022-04-13
DistributedNationwide (US)
Quantity100 units
Reason classessterility
Lot numbers20163461674, 20170461910, 20170462303, 20219463245, 20238464203, 20268464581, 21082472172, 21110472562, 21138473542, 21167474498, 21287478853, 21349479943
Model numbers570-2677

Product

Anterior Hip Pack - Surgical Kit

Reason for recall

The outer bag may be perforated or torn, which may result in a breach in the sterility of the kit.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0865-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.