ClearanceBrief
Recall Z-0974-2025 ยท BRY Cabinet, Table And Tray, Anesthesia

CareFusion 303, Inc.

BD Pyxis MedStation 4000 AUX, REF 306

DateJan 17, 2025 (initiated Feb 14, 2023)
StatusOpen, Classified
ReasonDrawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
Root causeNonconforming Material/Component
ActionBD issued an Urgent Medical Device Product Advisory to its consignees on 02/14/2023 via letter. The notice explained the problems with the device, health hazards, and requested the following actions be taken: "1. Customers may continue to use these devices as intended and should file a complaint via the Customer Portal at https://www.bd.com/self-service or call BD Support at 1-800-727-6102, should you experience drawer or door failures. 2. If you experience delays in access to medication due to a drawer or door failure, ensure backup procedures (which may include but may not necessarily be
Quantity5056 units
DistributionWorldwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.