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.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-1076-2025 | Allura CV20 System Code: 722031 | 119 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1077-2025 | Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026 | 474 units US; 1908 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1078-2025 | AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027 | 146 units US; 629 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1079-2025 | Allura Xper FD10C System Code: (1) 722001 | 1 unit OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1080-2025 | AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028 | 1528 units US; 3482 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1081-2025 | AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013 | 66 units US; 79 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1082-2025 | AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025 | 1 unit OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1083-2025 | AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035 | 1 unit US; 1 unit OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1084-2025 | AlluraXperFD20/10 System Code: (1) 722029 | 22 units US; 65 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1085-2025 | Allura Xper FD20/20 System Code: (1) 722038 | 33 units US; 82 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1086-2025 | AlluraXperFD20/15 System Code: (1) 722058 | 69 units US; 235 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1087-2025 | Azurion 3 M12 System Code: (1) 722063 (2) 722221 | 9 units US; 101 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1088-2025 | Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280 | 42 units US; 661 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1089-2025 | Azurion 5 M12 System Code: (1) 722227 (2) 722231 | 6 units US; 246 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1090-2025 | Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 722281 | 68 units US; 438 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1091-2025 | Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235 | 90 units US; 458 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1092-2025 | Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236 | 251 units US; 938 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1093-2025 | Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233 | 324 units US; 1390 units OUS | Class II | Ongoing | 12 Feb 2025 |
| Z-1094-2025 | Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) 722234 (4) 722282 System Code: (1) 722078 (2) 722223 (3) 722233 | 1346 units US; 2582 units | Class II | Ongoing | 12 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
Official channels
- FDA enforcement report Z-1076-2025The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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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.