# FDA recall Z-0367-2026 > **CareFusion 303, Inc.** · Class II · device recall initiated 2025-09-30. ## Product Various models of BD Pyxis Medbank: Reference numbers: 1137-00 1145-00 1146-00 1147-00 1148-00 138902-01 138903-01 138905-01 138906-01 138907-01 138908-01 138909-01 138910-01 138911-01 138912-01 138913-01 138914-01 138915-01 138916-01 138917-01 138918-01 138919-01 138920-01 138921-01 138922-01 138923-01 138924-01 138926-01 138927-01 138928-01 138929-01 138930-01 138931-01 138932-01 138933-01 138934-01 138936-01 138937-01 138938-01 138939-01 138940-01 138941-01 138942-01 138943-01 138944-01 138945-01 138946-01 138947-01 138948-01 138949-01 138950-01 138951-01 138952-01 138953-01 138954-01 138955-01 138956-01 138957-01 138958-01 138959-01 138960-01 138961-01 138962-01 138963-01 138964-01 138965-01 138966-01 138967-01 138968-01 138969-01 138970-01 138971-01 138972-01 138973-01 138974-01 138975-01 138976-01 138977-01 138978-01 138989-01 138990-01 139000-01 139001-01 139002-01 139011-01 139013-01 139016- ## Reason for recall Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire. ## Distribution Worldwide distribution - US Nationwide and the countries of Canada, United Arab Emirates, Australia. ## Key facts - **Recall number:** Z-0367-2026 - **Recalling firm:** CareFusion 303, Inc. - **Classification:** Class II - **Product type:** device - **Status:** Ongoing - **Initiation date:** 2025-09-30 - **Report date:** 2025-11-05 - **Voluntary/Mandated:** Voluntary: Firm initiated - **Location:** San Diego, CA, United States ## Primary source FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0367-2026 ## Citation > AI Analytics. FDA recall Z-0367-2026. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0367-2026. Source: US FDA. Licensed CC0. --- *[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*