Philips Allura and Azurion Patient Tables Recall Due to Finger Entrapment Risk
Philips is recalling AD7 and AD7X patient tables used in Allura and Azurion medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel are at risk of finger injury.
The agency’s classification
FDA (Devices): Class II
Class II is 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.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is a risk-of-harm product with a physical entrapment mechanism that could cause finger injuries to healthcare workers. Classified as FDA Class II with no reported hospitalizations or deaths documented in the source material, it meets the criteria for a High severity rating as a risk-of-harm product where injury has not been reported.
Plain-English summary
Philips is recalling the AD7 and AD7X patient tables (both tilt and non-tilt versions) that are used with Allura and Azurion medical imaging systems. The recall affects 22 units in the United States and 65 units in other countries worldwide.
During manual repositioning of the patient tabletop, fingers can become entrapped between the longitudinal guiding rails and the tabletop surface. This entrapment may result in finger injuries to healthcare workers, including operators and service personnel.
Healthcare facilities using these affected systems should be aware of this entrapment hazard. Personnel performing manual repositioning of the patient table should exercise caution to avoid finger entrapment between the guiding rails and tabletop.
The recalled product
- Product
- AlluraXperFD20/10 System Code: (1) 722029
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Category
- Medical Device
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- UDI: 00884838054219(21)
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 19 recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 19 products in this recall →Related recalls
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