{"url_path":"/fda/device/recalls/Z-2610-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Medline Convenience kits containing recalled Swan-Ganz Catheters    CV ANESTHESIA - ROOM SET UP\t  \tDYNJ905503D  \tDYNJ905503F  \tDYNJ905503G","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-28","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2610-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Medline Industries, LP"},"word_count":163,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2610-2026\n\n**Recalling firm:** Medline Industries, LP\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-28\n**Report date:** 2026-07-08\n\n## Product\nMedline Convenience kits containing recalled Swan-Ganz Catheters    CV ANESTHESIA - ROOM SET UP\t  \tDYNJ905503D  \tDYNJ905503F  \tDYNJ905503G\n\n## Reason\nKits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.\n\n## Affected lots\nDYNJ905503D    UDI-DI 10193489430295    lots 21DBG611   21EBI605   21FBN751  DYNJ905503F    UDI-DI 10193489967272    lots 21HBL060   21IBW859   22DBC340   22DBS437   22FBR267   22GBR286   22HBS560   22IBA577   22JBI883   22KBD587   22LBF425   23BBN903   23CBL450   23CBW776   23FBC209   23IBU343   24DBQ181   24FBT062   24GBR740   24HBI428   24JBP984  DYNJ905503G    UDI-DI 10198459200397    lots 25ABJ069   25ABL749   25CBB762   25DBG799   25EBM994   25GBW226   25LBA950   25LBT019   26ABH519   26ABT315   26BBQ338   26DBJ110\n\n## Distribution\nUS Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI."}