Data Foundry

Medical device recalls 2014

ACUSON SC2000 Power Input: 100-240VAC — Class II medical device recall Z-0825-2014

Terminated recall by Siemens Medical Solutions USA, Inc., reported 2014-02-05, distributed nationwide. The locking mechanism that is intended to hold the control panel in a fixed position can become loose and fail

Recall numberZ-0825-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSiemens Medical Solutions USA, Inc., Mountain View, CA, United States
Recall initiated2013-12-22
Classified2014-01-24
Reported by FDA2014-02-05
Terminated2015-03-05
DistributedNationwide (US)
Countries outside the USAE, AT, AU, CA, CN, DE, EC, ES, FI, FR, GB, IE, IL, IN, IT, JP, KR, MX, PH, PT, RS, SA, SE, TR, TW, ZA
Quantity271 units
Serial numbers401108, 401109, 401110, 401111, 401113, 401114, 401115, 401116, 401117, 401118, 401119, 401120, 401121, 401122, 401123, 401124, 401126, 401127, 401128, 401129, 401130, 401131, 401132, 401133, 401134 and 235 more
Model numbers10433816

Product

ACUSON SC2000 Power Input: 100-240VAC, 1600 Max 50/60Hz; Siemens Medical Solutions USA, Inc. 685 East Middlefield Road Mountain View, CA 94043 Ultrasound imaging system.

Reason for recall

The locking mechanism that is intended to hold the control panel in a fixed position can become loose and fail to lock the rotation of the control panel, making it unable to steer or control during transport.

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-0825-2014. 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.