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Recall Observatory FDA recall evidence

Device product

Dimension Vista Protein 1 Calibrator, PROT 1 CAL, Siemens Material Number (SMN) 10465664 (US) and 10469516 (OUS), Product Code KC710U (US) and KC710 (OUS); IVD

Z-0173-2018

May 23, 2017

Class II

Product summary

Firm
Siemens Healthcare Diagnostics, Inc.
Event
Event 77381
Status
Terminated
Classification
Class II
Quantity
N/A
Official record key
device-enforcement:Z-0173-2018

Official wording

Reason: Complaint of high amount of ceruloplasmin patient results below the reference range (< 20 mg/dL [0.2 g/L]. PROT1 CAL and corresponding PROT1 CON L, M, and H are inaccurately assigned for ceruloplasmin (CER).

Code information: Lot numbers: 6JC001, 6JC001C, 6JC001G (exp. date 2018-01-11); 6MC001, 6MC001C (exp. date 2018-04-29); 6CC001A, 6CC001B, 6CC001F (exp. date 2017-07-14); 6FC001A, 6FC001C, 6FC001E (exp. 2017-10-27); --- Lot # (UDI): 6CC001A (008427680244436CC001A20170714), 6CC001B (008427680244436CC001B20170714), 6CC001F (008427680244436CC001F20170714), 6FC001A (008427680244436FC001A20171027), 6FC001C (008427680244436FC001C20171027), 6FC001E (008427680244436FC001E20171027), 6JC001 (008427680244436JC00120180111), 6JC001C (008427680244436JC001C20180111), 6JC001G (008427680244436JC001G20180111), 6MC001 (008427680244436MC00120180429), 6MC001C (008427680244436MC001C20180429).

Distribution pattern: Worldwide Distribution - US (nationwide) Internationally to Austria, Australia, Belgium, Canada, France, Germany, Great Britain, Italy, Japan, Netherlands, Portugal, Slovakia, Spain, Switzerland and Republic of Korea South

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Complaint of high amount of ceruloplasmin patient results below the reference range (< 20 mg/dL [0.2 g/L]. PROT1 CAL and corresponding PROT1 CON L, M, and H are inaccurately assigned for ceruloplasmin (CER).