{"url_path":"/fda/device/recalls/Z-2919-2026","section_key":"summary","section_title":"DEVICE Recall: Covidien, LP — V-Loc 180 Absorbable Wound Closure Device    BOX BEDSIDE STAPLING IS KING\t  \tBOX06614V4  \t  BOX BY PASS FINAL\t  \tBOX07405V1  \t  BOX BYPASS CARDON\t  \tBOX01056V2\t  \t  BOX BYPASS DR LAGAE\t  \tBOX01482V2  \t\t  BOX BYPASS KIT DEZEMBER 2025\t  \tBOX09222V1  \t\t  BOX BYPASS KIT NEU BOX 003\t  \tBOX08767V1  \t  BOX GASTRIC BYPASS\t  \tJAWBYPASS2  \t  BOX GASTRIC BYPASS SIGNIA\t  \tBOX021…","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-06-24","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2919-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Covidien, LP"},"word_count":608,"has_tables":false,"body_markdown":null}