Recall Register

Device recall: Allura CV20 System Code: 722031

Class II FDA enforcement event 96120. Recall start date: . Status in the FDA record: Ongoing.

Reason for recall, in the words of FDA

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. started this device recall on 13 Jan 2025. The firm address in the FDA record is in Best. FDA put the recall in Class II. FDA event 96120 has 19 product records. The first FDA enforcement report date is 12 Feb 2025. The record gives the status Ongoing.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Worldwide distribution - US Nationwide and the countries of Canada, Afghanistan, Albania, Algeria, Argentina, Armenia, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belarus, Belgium, Bolivia,…

Recalling firm

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., Best, Netherlands.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

19 product records in the event.

FDA event 96120: product records
Recall numberProductQuantityClassStatusReport date
Z-1076-2025Allura CV20 System Code: 722031119 units OUSClass IIOngoing12 Feb 2025
Z-1077-2025Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026474 units US; 1908 units OUSClass IIOngoing12 Feb 2025
Z-1078-2025AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027146 units US; 629 units OUSClass IIOngoing12 Feb 2025
Z-1079-2025Allura Xper FD10C System Code: (1) 7220011 unit OUSClass IIOngoing12 Feb 2025
Z-1080-2025AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 7220281528 units US; 3482 units OUSClass IIOngoing12 Feb 2025
Z-1081-2025AlluraXper FD20 Biplane System Code: (1) 722008 (2) 72201366 units US; 79 units OUSClass IIOngoing12 Feb 2025
Z-1082-2025AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 7220251 unit OUSClass IIOngoing12 Feb 2025
Z-1083-2025AlluraXper FD20 OR Table System Code: (1) 722023 (2) 7220351 unit US; 1 unit OUSClass IIOngoing12 Feb 2025
Z-1084-2025AlluraXperFD20/10 System Code: (1) 72202922 units US; 65 units OUSClass IIOngoing12 Feb 2025
Z-1085-2025Allura Xper FD20/20 System Code: (1) 72203833 units US; 82 units OUSClass IIOngoing12 Feb 2025
Z-1086-2025AlluraXperFD20/15 System Code: (1) 72205869 units US; 235 units OUSClass IIOngoing12 Feb 2025
Z-1087-2025Azurion 3 M12 System Code: (1) 722063 (2) 7222219 units US; 101 units OUSClass IIOngoing12 Feb 2025
Z-1088-2025Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 72228042 units US; 661 units OUSClass IIOngoing12 Feb 2025
Z-1089-2025Azurion 5 M12 System Code: (1) 722227 (2) 7222316 units US; 246 units OUSClass IIOngoing12 Feb 2025
Z-1090-2025Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 72228168 units US; 438 units OUSClass IIOngoing12 Feb 2025
Z-1091-2025Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 72223590 units US; 458 units OUSClass IIOngoing12 Feb 2025
Z-1092-2025Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236251 units US; 938 units OUSClass IIOngoing12 Feb 2025
Z-1093-2025Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233324 units US; 1390 units OUSClass IIOngoing12 Feb 2025
Z-1094-2025Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) 722234 (4) 722282 System Code: (1) 722078 (2) 722223 (3) 7222331346 units US; 2582 unitsClass IIOngoing12 Feb 2025

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2025
945
Share of these events in Class II
85%
Product records in this event
19Median of the firm: 1
Events of the firm on the register
59

Other events of the firm

Other FDA enforcement events of PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
InitiatedProduct (first record)TypeClassRecords
16 Jul 2026Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222,722223, 722224, 72DeviceClass II1
16 Jul 2026Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232, 722233, 722234, 722235, and 722236, with Software VersioDeviceClass II1
29 Jun 2026Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopDeviceClass II1
17 Jun 2026Philips Allura under the following System Descriptions and corresponding model numbers: 1. Allura Xper FD10; Model NumbeDeviceClass II3
18 May 2026Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost Eleva; Model # 708034 forDeviceClass II2
30 Apr 2026Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222),DeviceClass II2
28 Apr 2026Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions anDeviceClass II1
28 Apr 2026Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (DeviceClass II3
31 Mar 2026Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, 722229), Azurion 3 M15 (722222, 722230),DeviceClass II1
19 Mar 2026Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device (Interventional Tool) intended to DeviceClass II1

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: all 59 events

Official channels

Cite this page

Recall Register. FDA enforcement event 96120. https://recallregister.com/fda/ii/96120/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA device enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Worldwide distribution - US Nationwide and the countries of Canada, Afghanistan, Albania, Algeria, Argentina, Armenia, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belarus, Belgium, Bolivia,…
What quantity of product is in FDA event 96120?
The event has 19 product records. The first record gives this quantity: 119 units OUS
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many device recalls of 2025 have the same class?
85% of the 945 device events that started in 2025 are in Class II.