CareFusion 303, Inc. recalls BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
Reason for recall
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Affected products & lots
- BD Pyxis Anesthesia Station ES REF: 327 Medication cabinetUDI 10885403477836
What the firm is doing
On April 30, 2026, CareFusion (subsidiary of Becton, Dickinson and Company) issued a Urgent Medical Device Recall Notification, via mail or Email. CareFusion ask consignees to take the following actions: 1. Dispensing cabinets can continue to be used as intended. 2. If you suspect that the Bio-ID Scanner is hot, please discontinue the use of Scanner and file a complaint. 3. Review and update facility policies and procedures related to situations where the Bio-ID Scanner is unavailable to mitigate delays in care. 4. Complete the attached Customer Response Form and return to the BD contact noted on the form.
DistributionShow detailsHide
US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-2299-2026
- FDA device classification · BRYOfficial FDA classification for this device type
- CFR regulation · 21 CFR 868.6100The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find CareFusion 303, Inc.Search for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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