Recall Z-1519-2011

Fisher Diagnostics, A Company of Fisher Scientific LLC · initiated October 6, 2010

Terminated

Product

Pacific Hemostasis Thromboplastin-DS, catalog #100354, packaged in 4 mL lypholyzed vials, 10 bottles/carton. Vials are labeled, in part ***Fisher Diagnostics a division of Fisher Scientific Company, LLC Middletown, VA 22645-1905 USA*** Thromboplastin-DS is a Class 2 medical device intended for use in performing the one stage prothrombin time (PT) test and PT-based factor assays.

Codes / lots: V40526, exp 4/2013 V40826, exp 4/2013

Reason for recall

An in vitro diagnostic reagent used in coagulation testing may cause inaccurate clotting times in quality control and patient plasma samples.

FDA-determined cause: Nonconforming Material/Component

Action taken

The firm, ThermoFisher Scientific, sent two "Urgent Medical Device Removal" letters one via Federal Express on October 20, 2010 and certified mail for domestic customers on October 21, 2010. The letters described the product, problem and action to be taken by the customers. The customers were instructed to indicate the quantities of all affected product currently in stock at their facility; complete and return the attached Response Form/table to Fisher Diagnostics via fax to (540) 869-8129 or by mail to the attention of Technical Support; dispose of any remaining inventory of the affected lot numbers; provide a copy of this letter to their customers, and file this letter for future reference. If you have any questions regarding this notification, please contact our Technical Support staff at 800-528-0494, Option 2, or email techsupport.diagnostics.mtn@themofisher.com.

Details

Recall number
Z-1519-2011
Initiated
October 6, 2010
Terminated
November 2, 2011
Product code
GJS – Test, Time, Prothrombin
Quantity
1190 kits
Distribution
Worldwide distribution: USA including states of: Alaska, Florida, Kentucky, Ohio, New Jersey, New York, and Texas; and countries including: Argentina, Dubai, Italy, Mexico, Philippines, Romania, and Turkey.
Recalling firm
Fisher Diagnostics, A Company of Fisher Scientific LLC, Middletown, VA

Official FDA recall record