Data Foundry

Medical device recalls 2015

Artis Q systems — Class II medical device recall Z-2341-2015

Terminated recall by Siemens Medical Solutions USA, Inc, reported 2015-08-12, distributed nationwide. The possibility exists for a large amount of liquid to seep through the top cover of the table and penetrate t

Recall numberZ-2341-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSiemens Medical Solutions USA, Inc, Malvern, PA, United States
Recall initiated2015-06-29
Classified2015-08-05
Reported by FDA2015-08-12
Terminated2016-12-07
DistributedNationwide (US)
Serial numbers109007, 109009, 109010, 109011, 109015, 109016, 109020, 109021, 109027, 111000, 121004, 121006, 121008, 121009, 121010, 121011, 121012, 121013, 121014, 121015, 121016, 121018, 121019, 121020, 121036 and 7 more

Product

Artis Q systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography, general angiography, rotational angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures.

Reason for recall

The possibility exists for a large amount of liquid to seep through the top cover of the table and penetrate the components inside the table. If this occurs, table movements may no longer be possible. No injuries reported.

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-2341-2015. 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.