Events

Recall of Device Recall N PROT STANDARD SL

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by CSL Behring GmbH.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    77515
  • Event Risk Class
    Class 2
  • Event Number
    Z-0190-2018
  • Event Initiated Date
    2017-06-05
  • Event Status
    Open, Classified
  • Event Country
    United States
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=156195
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Immunochemical, ceruloplasmin - Product Code CHN
  • Reason
    Siemens healthcare diagnostics has confirmed a negative bias of approximately -20% for results obtained with n antiserum to human ceruloplasmin when calibrating ceruloplasmin with various lots of n protein standard sl. n/t protein controls sl for ceruloplasmin are similarly biased. --- the affected standards and controls for the affected lots were incorrectly value assigned, which led to a lower result compared to correctly assigned standards. note: n antiserum to human ceruloplasmin (ref ouie) works as intended. --- siemens investigation indicated that n protein standard sl and corresponding n/t protein control sl (levels low, mid and high) are inaccurately assigned for ceruloplasmin.
  • Action
    URGENT MEDICAL DEVICE CORRECTION Letter (PP17-011.a.US, dated May 30, 2017) was sent to US consignees via FedEx on 6/5/2017. URGENT FIELD CORRECTIVE ACTION Letter was e-mailed to customers Outside the US. Customers are instructed to use the re-assigned Ceruloplasmin values for the lots indicated in the letter.

Device

Device Recall N PROT STANDARD SL
  • Model / Serial
    Lot Numbers(UDI): 083611A (00842768007590083611A20170711),  083611B (00842768007590083611B20170711),  083611C (00842768007590083611C20170711),  083611D (00842768007590083611D20170711), exp. date 2017-07-11;  083612 (0084276800759008361220171014),  083612A (00842768007590083612A20171014), 083612B (00842768007590083612B20171014), exp. date 2017-10-14; 083614A (00842768007590083614A20180127),  083614B (00842768007590083614B20180127), 083614C (00842768007590083614C20180127), exp. date 2018-01-27; 083615 (0084276800759008361520180411),  083615A (00842768007590083615A20180411),  083615B (00842768007590083615B20180411),  083615C (00842768007590083615C20180411), exp. date 2018-04-11;  083616B (00842768007590083616B20180730),  083616C (00842768007590083616C20180730),  083616D (00842768007590083616D20180730), exp. date 2018-07-30.
  • Product Classification
    Immunology and Microbiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide including the countries of United States, Argentina, Australia, Austria, Bahrain, Bangladesh, Belgium, Bosnia-Herzegovina, Brazil, Bulgaria, Canada, Chile, China, Costa Rica, Croatia, Czech Republic, Cyprus, Denmark, Egypt, Finland, France, Germany, Greece, Great Britain, Hungary, India, Indonesia, Iraq, Ireland, Israel, Italy, japan, Kazakhstan, Kuwait, Latvia, Lebanon, Luxembourg, Macedonia, Mexico, Morocco, Netherlands, New Zealand, Norway, Poland, Portugal, Republic of Korea (S), Romania, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, Spain, Sweden, South Africa, Switzerland, Syria, Taiwan, Thailand, Trinidad-Tobago, Turkey, Turkmenistan, United Arab Emirates, Uruguay, Vatican, Venezuela,
  • Product Description
    SIEMENS N Protein Standard SL, for use on the BN II, BN ProSpec Systems, REF/Product Code OQIM 13, Siemens Material Number (SMN)10446073
  • Manufacturer
    CSL Behring GmbH

Manufacturer

CSL Behring GmbH
  • Manufacturer Address
    CSL Behring GmbH, Emil-von-Behring-Str. 76, Marburg Germany
  • Manufacturer Parent Company (2017)
    CSL Limited
  • Source
    USFDA