Philips AD7 and AD7X patient tables recalled due to finger entrapment risk
Philips has recalled the AD7 and AD7X patient tables used in medical imaging systems because fingers can become entrapped between the tabletop and guiding rails during manual repositioning, potentially causing injury.
What this means for you
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 Class II recall affecting a risk-of-harm medical device (patient tables) where finger entrapment can occur during normal use. No reported injuries or deaths have been documented. Per the severity rubric, risk-of-harm products where injury has not yet been reported receive a High severity score.
Plain-English summary
Philips Medical Systems Nederland B.V. has recalled the AD7 and AD7X patient tables (both tilt and non-tilt versions), which are components of Philips Allura Xper FD10 and Azurion medical imaging systems.
The recall addresses a potential safety issue with manual repositioning of the patient tabletop. During repositioning, a finger can become entrapped between the longitudinal guiding rails and the tabletop, which may result in finger injury. Both medical device operators and service personnel are at risk of this injury.
Approximately 474 units of the affected tables were distributed in the United States, and approximately 1,908 units were distributed internationally. These systems have been distributed worldwide to more than 100 countries.
The FDA has classified this as a Class II recall. Healthcare facilities with affected equipment should contact Philips Medical Systems for information regarding this recall and any available corrective actions.
The recalled product
- Product
- Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Category
- Medical Device — Patient Table
- Hazard
- finger-entrapment
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 (3)
- UDI: (1) 722003 00884838059191(10)
- (2) 722010 00884838059030(21)
- (3)722026 00884838054189(21).
Distribution
Distributed nationwide across the United States.
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