Z-2306-2016Class II

UroDiagnost; x-ray system

Name: Z-2306-2016 UroDiagnost; x-ray system
Creator: Philips Electronics North America Corporation
Published: 2016-07-19
License: https://open.fda.gov/license/

Philips North America LLC / initiated 2016-07-19 / Terminated / root cause: design

FDA source

Philips Electronics North America Corporation began a recall of UroDiagnost; x-ray system. Product Code: 708033 on 2016-07-19. FDA classified it as Class II and gives the reason as "The two bolts that attach the clamping plate to the lateral shaft may break, which could cause the c-arm to move laterally forward, slide out of its bearings, and sag". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-2306-2016
Classification: Class II
Status: Terminated
Initiated: 2016-07-19
Posted: 2016-08-01
Terminated: 2020-10-08
Recalling firm: Philips North America LLC
Product: UroDiagnost; x-ray system. Product Code: 708033
Product code: IXR Table, Radiographic, Tilting
Reason for recall: The two bolts that attach the clamping plate to the lateral shaft may break, which could cause the c-arm to move laterally forward, slide out of its bearings, and sag
Root cause tag: design
FDA root cause: Device Design
Action: On July 19, 2016, Philips sent a Field Safety Notice to all affected customers. Philips Field Service Engineers will add an independent safety catch free of charge.
Quantity in commerce: 993 total
Distribution: Worldwide distribution. US nationwide, Canada, Algeria, ARGENTINA, Australia, Austria, Belgium, China, Colombia, Czech Republic, Denmark, Egypt, Estonia, Faroe Islands, Finland, France, French Guiana, Germany, Greece, Hong Kong, Indonesia, Ireland, Israel, Italy, Jersey, Jordan, Republic of Korea, Latvia, Lebanon, Luxembourg, Malaysia, Mexico, Netherlands, New Zealand, Norway, Oman, Philippines, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Syrian Arab Republic, Taiwan, Thailand, TURKEY, Ukraine, United Arab Emirates, and United Kingdom.
Product codes and lots: All serial numbers. 708033 System serial numbers 1, 17, 15, 4, 3, 7, 18, 21, 8, 13, 14, 11, 5, 16, 2.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2306-2016
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2305-2016	Class II	Terminated	Voluntary: Firm initiated	2016-08-10	2016-08-01
Z-2306-2016	Class II	Terminated	Voluntary: Firm initiated	2016-08-10	2016-08-01
Z-2307-2016	Class II	Terminated	Voluntary: Firm initiated	2016-08-10	2016-08-01

Product code IXR

K911098Class IIPhilips Uro Diagnost MrfPhilips Medical Systems, Inc. / cleared 1991-07-03

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)