Philips Diagnost Stationary Radiographic System Models: 712020 — Class II medical device recall Z-1448-2013

Terminated recall by Philips Healthcare Inc., reported 2013-06-26, distributed nationwide. Installation Acceptance Test Document (IATD) non compliant with regulations. Records shows table height measur

Recall number	`Z-1448-2013`
Product type	Medical device
Classification	Class II
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	Philips Healthcare Inc., Andover, MA, United States
Recall initiated	2013-01-16
Classified	2013-06-17
Reported by FDA	2013-06-26
Terminated	2016-09-30
Distributed	Nationwide (US)
Countries outside the US	CA
Quantity	101 units
Reason classes	specification failure
Serial numbers	`316235`, `321739`, `334582`, `335517`, `344896`, `351321`, `356953`, `357879`, `359449`, `359767`, `363674`, `365639`, `365640`, `368428`, `372848`, `373499/SN0802249`, `373508`, `375366`, `375601/SN0802006`, `381098/SN0802124`, `381883/SN0802010`, `382018/SN0802118`, `382140/SN0702475`, `383639/SN0802099`, `386784/SN0802264` and 76 more
Model numbers	`712020`, `712022`, `712050`, `712052`, `712055`, `712057`, `712062`

Product

Philips Diagnost Stationary Radiographic System Models: 712020, 712022, 712050, 712052, 712055, 712057, 712062 Product Usage: Universal RAD Applications

Reason for recall

Installation Acceptance Test Document (IATD) non compliant with regulations. Records shows table height measurements out of specification with the consequence of potential system mis-alignment.

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-1448-2013. 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.