Cl Il Bio-Rad Variant II TURBO

Company:Bio-Rad Laboratories, Inc.
Date of Enforcement Report 4/1/2009
Class:ll

PRODUCT
Bio-Rad Variant II TURBO Hemoglobin Testing System with CDM v 4.0, model number 270-2600. Provides an integrated method for sample preparation, separation and the percent determination of percent hemoglobin A 1 c in EDTA human whole blood. This device only tests for A 1 c, Recall # Z-1041-2009

REASON
Sample results may be assigned to the wrong barcode number and tube position numbers, leading to discrepant sample results.

RECALLING FIRM/MANUFACTURER
Bio-Rad Laboratories, Inc., Hercules, CA, by letter, fax and telephone on October 17, 2008. Firm initiated recall is ongoing.

VOLUME OF PRODUCT IN COMMERCE
92 units

DISTRIBUTION
Nationwide and Internationally

About the author

Amy enjoys researching and writing about developments in medical technology and how that intersects with US law. She received her J.D. from the University of Florida Levin College of Law in 2020 and now works as a Regulatory Associate for SoftwareCPR®, a general-purpose regulatory consulting firm that is recognized globally for their expertise with standards and national regulations pertaining to medical device, mobile medical app, and HealthIT software.

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Corporate Office

15148 Springview St.
Tampa, FL 33624
USA
+1-781-721-2921
Partners located in the US (CA, FL, MA, MN, TX) and Canada.