Data Foundry

Medical device recalls 2025

Philips Azurion 7M20 systems with FlexArm ceiling-mounted system — Class II medical device recall Z-0719-2026

Ongoing recall by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., reported 2025-12-03, distributed in AL, AR, AZ, CA, CO, FL, GA, HI…. The motorized longitudinal movement of the FlexArm stand may be inconsistent (not smooth) and eventually may b

Recall numberZ-0719-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmPHILIPS MEDICAL SYSTEMS NEDERLAND B.V., Best, N/A, Netherlands
Recall initiated2025-10-02
Classified2025-11-26
Reported by FDA2025-12-03
DistributedAL, AR, AZ, CA, CO, FL, GA, HI, IL, IN, KS, KY, MD, MN, MO, NM, NY, OH, OK, PA, RI, TX, UT, VA, WA, WI, WV, WY
Countries outside the USAT, AU, BE, BG, CA, CH, CZ, DE, DK, ES, FI, FR, GB, HK, IQ, IT, JP, KR, NL, NO, PH, PL, RO, SE, TH, VN, ZA
Quantity172 units
Reason classespackaging
Model numbers722234

Product

Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;

Reason for recall

The motorized longitudinal movement of the FlexArm stand may be inconsistent (not smooth) and eventually may become unavailable. This issue is due to grease leakage from the bearings and/or anti-corrosion oil applied on the bearings, because of which the lubrication on the ceiling rail may be excessive, reducing the friction between the rails and the friction wheel. Expansion to add additional model.

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-0719-2026. 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.