FDA Device recall Z-1807-2015
Philips Ultrasound, Model Q-Station, with software version 3 or higher, Catalog number: 795088
- FDA Device
- Class II
- terminated
- Published 2015-06-24
On 2015-06-24 the FDA classified a Class II recall of Philips Ultrasound, Model Q-Station, with software version 3 or higher, Catalog number: 795088 by Philips Ultrasound, citing philips Healthcare has discovered a problem in the Philips Ultrasound Q-Station version 3.0 or higher that could result in measurements from a study (Structured Report) to be appe….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1807-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-05-15 |
| Published | 2015-06-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Philips Ultrasound |
| Distribution | US |
Product
Philips Ultrasound, Model Q-Station, with software version 3 or higher, Catalog number: 795088; Part Number: 989605382391 Q-Station is application software intended to manage, view, analyze, and report qualitative and quantitative image data from ultrasound exams. It is designed to host optional advanced analysis applications via QLAB integration and provide integrated tools that allow users to manually assess and score cardiac wall motion and export images and / or exams and reports. Q-Station can view DICOM images of non-ultrasound images such as CT, MR, NM, CR, MG, XA, PET, RT and X-Ray modalities for reference viewing. It support connectivity to ultrasound systems, PACS and other DICOM storage repositories.
Reason
Philips Healthcare has discovered a problem in the Philips Ultrasound Q-Station version 3.0 or higher that could result in measurements from a study (Structured Report) to be appended to subsequent studies for other patients.
Identifiers
| code_info | *****************US Serial numbers***************************************** 2176-IAF08E60-15D4, 2187-VAC5T6CD-157D,…*****************US Serial numbers***************************************** 2176-IAF08E60-15D4, 2187-VAC5T6CD-157D, 2C98-25A23E3A-4B2E, 34F5-4084F543-80EA, 3A5D-4079F60B-80D4, 54B0-HADF24F2-15B1, 678B-NAE42F41-15BB, 6FF9-259B5EB7-4B20, 725B-GACE30D1-158F, 72EE-408914F8-80F2, 7A39-497627F7-92C9, 8536-IAD33B20-1599, A584-QAE84EF6-15C3, A838-IAE2CF5A-15B8, B903-407CB5D9-80D9, BDC7-TAE25A0D-15B7, D356-YAE1E4C0-15B6, D60A-GADC6524-15AB, D8BE-KAD6E588-15A0, DB72-RAD165EC-1595, DE26-WACBE650-158A, E0DA-XAC666B4-157F, E16D-40814ADB-80E2, E8E5-TAE16F73-15B5, EE4D-IAD6703B-159F, F669-PAC5F167-157E, F90C-MAEBF95E-15CA, H944-VACAFBB6-1589, MBF8-WAC57C1A-157E, U9D7-4085DFDD-80EC. ********************Serial numbers in CANADA**************************************** 1ED3-QACA8669-1588, 4489-SAD49B07-159C, B054-UAD25086-1597, C897-TACC5B9D-158B, and F3B5-IACB7103-1589. *********************Serial numbers in other countries*********************************** 114F-Q |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1807-2015%22
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