MalfunctionFSM

ACTIS

Received Jul 27, 2026 · Event occurred Jun 29, 2026

Report 1818910-2026-12571 · MDR key 50005317

Device

Generic name

Instrument Cases

Manufacturer

Depuy Orthopaedics Inc Us

Catalog number

201004200

Product problems

Peeled/Delaminated

Patient

Unknown

No Clinical Signs, Symptoms or Conditions