{"url_path":"/fda/device/recalls/Z-2702-2026","section_key":"summary","section_title":"DEVICE Recall: Fresenius Medical Care Holdings, Inc. — 5008X Blood Tubing Set, 24 units per case. Includes the below model numbers and descriptions.    1. 5008X HD Pre-Flush   Standard Blood Tubing Set; Model Number: 03-5110-6.    2. 5008X HD Pre-Flush   With Twister Blood Tubing Set; Model Number: 03-5160-1.     3. 5008X HD/HDF   Standard Blood Tubing Set; Model Number: 03-5300-3.     4. 5008X H…","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-11","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2702-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Fresenius Medical Care Holdings, Inc."},"word_count":198,"has_tables":false,"body_markdown":null}