Data Foundry

Medical device recalls 2017

FV-RF — Class II medical device recall Z-1005-2017

Terminated recall by Philips Medical Systems (Cleveland) Inc, reported 2017-01-18, distributed nationwide. There's a potential for liquid penetration into the back side of the front control panel of the X-ray diagnost

Recall numberZ-1005-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmPhilips Medical Systems (Cleveland) Inc, Cleveland, OH, United States
Recall initiated2016-11-18
Classified2017-01-11
Reported by FDA2017-01-18
Terminated2018-07-02
DistributedNationwide (US)
Quantity41
Reason classesdevice malfunction
Serial numbers0162A65301, 0162A65401, 0162A65402, 0162A66005, 0162A66104, 0162A66105, 0162P21004, 0162R15403, 0162R15504, 0162R15602, 0162R15603, 0162R15702, 0162R15802, 0162R15803, 0162R15804, 0162R16001, 0162R16002, 0162R16003, 0162R16004, 0162R16007, 209669, 209677, 212866, 217296, 217530 and 5 more

Product

FV-RF (Clinix RF Plus) Product Usage: A Stationary X-ray System, a device intended for radiographic/fluoroscopic examinations of various anatomical regions. This device may include signal analysis and display equipment, patient and equipment supports, components and accessories.

Reason for recall

There's a potential for liquid penetration into the back side of the front control panel of the X-ray diagnostic table, which can cause a short circuit of the terminals of the tilt operation and cause an unintentional tilt of the table.

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-1005-2017. 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.