AlluraXper FD20 Biplane OR Table System Code: — Class II medical device recall Z-1082-2025

Ongoing recall by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., reported 2025-02-12, distributed nationwide. Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Phil

Recall number	`Z-1082-2025`
Product type	Medical device
Classification	Class II
Status	Ongoing
Voluntary or mandated	Voluntary
Recalling firm	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., Best, Netherlands
Recall initiated	2025-01-13
Classified	2025-02-04
Reported by FDA	2025-02-12
Distributed	Nationwide (US)
Countries outside the US	AE, AF, AR, AT, AU, BD, BE, BG, BH, BO, BR, CA, CH, CL, CN, CO, CR, CY, CZ, DE, DK, DO, DZ, EC, EE, EG, ES, FI, FR, GB, GH, GR, GT, HK, HN, HR, HU, ID, IE, IL, IN, IQ, IR, IS, IT, JM, JO, JP, KE, KR, KW, KY, LB, LK, LT, LV, MA, MT, MX, MY, NG, NI, NL, NO, NP, NZ, OM, PA, PE, PH, PK, PL, PT, PY, QA, RO, RS, SA, SE, SG, SI, SK, TH, TN, TR, TT, TW, UA, UY, VE, VN, ZA
Quantity	1 units

Product

AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1082-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.