Data Foundry

Medical device recalls 2015

e — Class II medical device recall Z-0914-2015

Terminated recall by Siemens Medical Solutions USA, Inc., reported 2015-01-14, distributed nationwide. There is a potential for patient finger injury on the e.cam systems.

Recall numberZ-0914-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSiemens Medical Solutions USA, Inc., Hoffman Estates, IL, United States
Recall initiated2014-04-08
Classified2015-01-06
Reported by FDA2015-01-14
Terminated2016-12-23
DistributedNationwide (US)
Countries outside the USAE, AR, AT, AU, BD, BE, BG, BH, BO, BR, CA, CH, CL, CN, CO, CR, CZ, DE, DK, DZ, EC, EG, ES, FI, FR, GB, GH, GR, HK, HN, HR, ID, IE, IL, IN, IQ, IR, IT, JM, JO, JP, KR, KW, LB, LK, LU, LV, MA, MX, MY, NG, NL, NO, NP, NZ, OM, PE, PH, PK, PL, PT, QA, RO, RS, SA, SE, SG, SI, SK, SV, TH, TN, TR, TT, TW, UA, UY, VN, ZA
Quantity4,462 systems
Serial numbers01009R, 05173/5992099, 08501/7823920, 10000, 10001, 10002, 10004, 10005, 10006, 10007, 10008, 10009, 1001, 10010, 100100018, 10011, 10012, 10013, 10014, 10015, 10016, 10017, 10018, 10019, 1002 and 475 more

Product

e.cam -emission computed tomography system Used to detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588keV.

Reason for recall

There is a potential for patient finger injury on the e.cam systems.

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-0914-2015. 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.