Allura Xper FD20 Biplane OR Table — Class II medical device recall Z-0007-2026

Ongoing recall by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., reported 2025-10-08, distributed nationwide. The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is de

Recall number	`Z-0007-2026`
Product type	Medical device
Classification	Class II
Status	Ongoing
Voluntary or mandated	Voluntary
Recalling firm	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., Best, N/A, Netherlands
Recall initiated	2025-09-03
Classified	2025-10-01
Reported by FDA	2025-10-08
Distributed	Nationwide (US)
Countries outside the US	AE, AR, AT, AU, BD, BE, BG, BO, BR, CA, CH, CL, CN, CO, CR, CW, CY, CZ, DE, DK, DO, DZ, EC, EE, EG, ES, FI, FR, GB, GR, HN, HR, HU, ID, IE, IL, IN, IQ, IR, IT, JM, JO, JP, KE, KR, LB, LK, LT, LV, MA, MT, MX, MY, NL, NO, NP, NZ, PA, PE, PH, PL, PT, PY, RO, RS, SA, SE, SG, SI, SK, TH, TN, TR, TT, TW, UA, UY, VE, VN, ZA
UPC / GTIN / UDI-DI	`00884838059108`
Model numbers	`00884838059108`, `722020`, `722025`

Product

Allura Xper FD20 Biplane OR Table; Model Numbers: (1) 722020, (2) 722025; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

Reason for recall

The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages are shown before the battery is low on power or depleted.

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-0007-2026. 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.