{"url_path":"/fda/device/recalls/Z-2299-2026","section_key":"summary","section_title":"DEVICE Recall: CareFusion 303, Inc. — BD Pyxis Anesthesia Station ES  REF: 327  Medication cabinet","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-30","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2299-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"CareFusion 303, Inc."},"word_count":80,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2299-2026\n\n**Recalling firm:** CareFusion 303, Inc.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-30\n**Report date:** 2026-06-10\n\n## Product\nBD Pyxis Anesthesia Station ES  REF: 327  Medication cabinet\n\n## Reason\nFingerprint scanner may overheat to a temperature  to cause 1st degree burn.\n\n## Affected lots\nAll Serial Numbers/UDI:10885403477836\n\n## Distribution\nUS: Nationwide  OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW"}