Data Foundry

Medical device recalls 2017

Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment… — Class II medical device recall Z-1020-2017

Terminated recall by Stryker Howmedica Osteonics Corp., reported 2017-01-18, distributed nationwide. Reunion TSA Peg Alignment Sound broke during surgery.

Recall numberZ-1020-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmStryker Howmedica Osteonics Corp., Mahwah, NJ, United States
Recall initiated2016-12-02
Classified2017-01-12
Reported by FDA2017-01-18
Terminated2018-08-01
DistributedNationwide (US)
Quantity131 units
Model numbers5901-1038

Product

Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment Sound (PIN 5901-1038, Revision A) is an instrument used in the ReUnion TSA shoulder system for confirming seating height and peg alignment of the TSA Self-Pressurizing Polyethylene Glenoid implant prior to final implantation into the glenoid vault. Its purpose is to provide assurance that the drilled holes for seating of the Glenoid implant have been properly prepared using the provided instrumentation

Reason for recall

Reunion TSA Peg Alignment Sound broke during surgery.

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-1020-2017. 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.