Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography (CT) X-ray System.
FDA Recall Z-1041-2026 · Posted 2026-01-09
Recalling FirmMobius Imaging, LLC
Recall StatusOpen, Classified
Product CodeJAK
Date Initiated2025-12-04
Product Quantity26 units
Reason for Recall
AIRO pendant replacement kits and upgrade do not possess the "Safe Hand Position Warning" label.
Firm Action
An URGENT MEDICAL DEVICE CORRECTION notice dated 12/4/25 instructs consignees to ensure the following mitigations are in place while the correction is deployed: the hand position warnings as indicated in the IFU, train operators, the AIRO is accessible through a physical key switch and password protected log in screen, and the Backing Up System Warning label is affixed on to the gantry of affected devices. Stryker will correct devices during an upcoming service visit. Consignees are to inform users of devices of this recall by sharing the recall notice, immediately check stock areas and operating rooms to identify affected devices, and inform all users of the potential harms and their risk mitigations. Consignees with any questions are to contact their local sales office or Stryker Representative.
Root Cause
Labeling Change Control
Distribution Pattern
US Nationwide distribution in the states of AK, AL, AZ, CA, CO, CT, DC, FL, IL, KY, MA, MD, MI, MN, MO, NC, NY, OH, PA, RI, SC, TN, TX, UT, VA, WI.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.