Recall Z-1228-2025 ยท BRY Cabinet, Table And Tray, Anesthesia
CareFusion 303, Inc.
155288-01 BD PYXIS MEDBANK MINI 1FH-1FM 169-137 BD PYXIS MEDBANK MINI 1FH-1FM 155311-01 BD PYXIS MEDBANK MINI 1FH-2HH 138921-01 BD PYXIS MEDBANK MINI 1HH-1FH-1HM 155159-01 BD PYXIS MEDBANK MINI 1HH-1FH-1HM 169-101 BD PYXIS MEDBANK MINI 1HH-1FH-1HM 139122-01 BD PYXIS MEDBANK MINI 1HH-1HM-1FM 155160-01 BD PYXIS MEDBANK MINI 1HH-1HM-1FM 169-102 BD PYXIS MEDBANK MINI 1HH-1HM-1FM 138912-01 BD PYXIS MED
| Date | Feb 21, 2025 (initiated Jan 8, 2025) |
| Status | Open, Classified |
| Reason | Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms. |
| Root cause | Under Investigation by firm |
| Action | On January 8, 2025, CareFusion 303 issued a "Urgent: Medical Device Correction" Notification to affected customer via mail or Email. CareFusion asked consignees to take the following actions: 1. Customers should immediately ensure that MedBank" devices are not installed in the procedural or operating space and at least 1.5 meters from patients. 2. Report any issues associated with the above products to BD Pyxis" MedBank" Product Support Line via phone at 866-930-9251. 3. Report any adverse health consequences experienced with the use of this product to the FDA's MedWatch Adverse Event Rep |
| Distribution | US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.