ClearanceBrief
Recall Z-2893-2026 ยท OWB Interventional Fluoroscopic X-Ray System

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System.

DateAug 5, 2026 (initiated Jun 17, 2026)
StatusOpen, Classified
ReasonPotential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
Root causeUnder Investigation by firm
ActionPhilips notified consignees on about 06/17/2026 via letter sent certified mail titled, URGENT Medical Device Correction. Consignees were instructed to circulate the notification letter to all users of the system for awareness and to follow the instructions. In the case motorized movements are unavailable, the stand can be manually repositioned using the handgrips and brake controls located on both sides of the stand. For ceiling-mounted systems, manual longitudinal (1), transversal (2) and rotational (3) stand movements remain available. Note: Transversal stand movements (2) are only available
Quantity257 units
DistributionUS Nationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K102005ALLURA XPER OR TABLE SERIES
Philips Medical Systems North America, Inc., Aug 9, 2010
K130638ALLURACLARITY XPER FD SERIES X-RAY SYSTEM
Philips Medical Systems Nederland B.V., Jun 28, 2013
K130842ALLURA XPER FD OR TABLE SERIES; ALLURA XPER FD10 SERIES; ALLURA XPER FD20 SERIES; ALLURA XPER FD BIPLANE SERIES
Philips Medical Systems Nederland B.V., May 21, 2013
K133292ALLURA XPER FD; OR TABLE
Philips Medical Systems Nederland B.V., Mar 5, 2014
K141979ALLURA XPER FD SERIES / ALLURA XPER OR TABLE SERIES
Philips Medical Systems Netherland BV, Aug 19, 2014
K161563Allura Xper FD series and Allura Xper OR Table series
Philips Medical Systems Nederland B.V., Jul 29, 2016