Recall Z-1230-2025— CareFusion 303, Inc.

Name: FDA recall Z-1230-2025
Creator: U.S. Food and Drug Administration
Published: 2025-01-08

Class II · Ongoing

Class II FDA medical device recall by CareFusion 303, Inc., initiated 2025-01-08. FDA's recall record names no specific 510(k) clearance for this event. Product: 139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK MINI 1FH-2HH MEDPASS 169-152 BD PYXIS MEDBANK MINI 2HH-1FM MEDPASS 169-150 BD PYXIS MEDBANK MINI 4HH MEDPASS 169-140 BD PYXIS MEDBANK TWR MN 3FH-8HH MEDPASS. Reason: Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms..

Recalling firm: CareFusion 303, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2025-01-08
Firm location: San Diego, CA, United States

Product description

139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK MINI 1FH-2HH MEDPASS 169-152 BD PYXIS MEDBANK MINI 2HH-1FM MEDPASS 169-150 BD PYXIS MEDBANK MINI 4HH MEDPASS 169-140 BD PYXIS MEDBANK TWR MN 3FH-8HH MEDPASS

Reason for recall

Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.

Data sourced from openFDA. This site is unofficial and independent of the FDA.