Data Foundry

Medical device recalls 2018

Allura Xper F010 DR Table — Class II medical device recall Z-3233-2018

Terminated recall by Philips Electronics North America Corporation, reported 2018-10-03, distributed nationwide. There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from t

Recall numberZ-3233-2018
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmPhilips Electronics North America Corporation, Andover, MA, United States
Recall initiated2018-07-16
Classified2018-09-21
Reported by FDA2018-10-03
Terminated2022-11-18
DistributedNationwide (US)
Countries outside the USAE, AR, AT, AU, BD, BE, BR, CA, CH, CL, CN, CY, CZ, DE, DK, DZ, EE, EG, ES, FI, FR, GB, GR, GT, HK, HR, HU, ID, IE, IL, IN, IR, IT, JO, JP, KE, KR, KW, LB, LK, LT, LV, MA, MT, MX, MY, NL, NO, NZ, OM, PE, PH, PK, PL, PT, RO, RS, RU, SA, SE, SG, SK, TH, TN, TR, TW, UA, VE, VN, ZA
Quantity5,115 total
Reason classesdevice malfunction

Product

Allura Xper F010 DR Table, System Code 722014 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging applications including diagnostics, Non-vascular interventions

Reason for recall

There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a Monitor Ceiling Suspension detaches from the actuator rotor shaft and the monitor falls, there is a risk of injury for the patient, user and bystander.

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-3233-2018. 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.