{"url_path":"/fda/device/recalls/Z-2528-2026","section_key":"summary","section_title":"DEVICE Recall: Zimmer, Inc. — Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide  Model/Catalog Number: 110040241","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-20","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2528-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Zimmer, Inc."},"word_count":107,"has_tables":false,"body_markdown":null}