InjuryKWS
COMPR SRS IC SEG - 90MM
Received Jul 30, 2026 · Event occurred Jul 3, 2026
Report 0001825034-2026-02220 · MDR key 50089746
Device
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
Not reported
- Insufficient Information
Narrative
Description of Event or Problem
It was reported patient underwent a revision post implantation due to unknown reason.Attempts have been made and no further information has been provided.
Additional Manufacturer Narrative
(b)(4).D10:Item # Unknown, Unknown Distal Humeral Component, Lot # Unknown.Item # Unknown, Unknown Humeral Head, Lot # Unknown.Item # Unknown, Unknown Proximal Humeral Component, Lot # Unknown.Item # Unknown, Unknown Assembly, Lot # Unknown.Product has been received by Zimmer Biomet and the investigation is in process. Once the investigation has been completed, a Follow-up MDR will be submitted.