{"url_path":"/fda/device/recalls/Z-1982-2026","section_key":"summary","section_title":"DEVICE Recall: Becton Dickinson & Co. — BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-07","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1982-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Becton Dickinson & Co."},"word_count":99,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-1982-2026\n\n**Recalling firm:** Becton Dickinson & Co.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-07\n**Report date:** 2026-05-06\n\n## Product\nBD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use\n\n## Reason\nBD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide levels below specification.\n\n## Affected lots\nCatalog Nunber: 260684; UDI-DI: 30382902606841; Lot Numbers: 5303157, 5329857, 5329860.\n\n## Distribution\nWorldwide distribution - US Nationwide and the country of Hong Kong."}