RecallRadar

FDA Device recall Z-1020-2017

Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment Sound (PIN 5901-1038, Revision A) is an instrument used in the ReUnion…

On 2017-01-18 the FDA classified a Class II recall of Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment Sound (PIN 5901-1038, Revision A) is an instrument used in the ReUnion… by Stryker Howmedica Osteonics, citing reunion TSA Peg Alignment Sound broke during surgery.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1020-2017
ClassificationClass II
Statusterminated
Initiated2016-12-02
Published2017-01-18
Last updated2026-09-13 11:54 UTC
CompanyStryker Howmedica Osteonics
DistributionUS

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

Reunion TSA Peg Alignment Sound broke during surgery.

Identifiers

code_infoCatalog #5901-1038

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1020-2017%22

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