Recall Z-2178-2011

Beckman Coulter Inc. · initiated December 17, 2009

Terminated

Product

Beckman Coulter Access Free T3 Calibrators, Part Number A13430 in vitro diagnostic.

Codes / lots: Lot #'s: 989902, 989903, 989904, 989905, 989906 & 989907

Reason for recall

Beckman Coulter has confirmed reports that the Access Free T3 calibrator lot numbers 989902, 989903, 989904, 989905, 989906 and 989907 will show a decline in performance before reaching their stated expiration date. The affected calibrator lots will cause one or more quality control samples to produce out-of-range high result.

FDA-determined cause: Nonconforming Material/Component

Action taken

Beckman Coulter sent a letter dated December 29, 2009, providing the customers with an explanation of the reason for recall and asked them to take the following actions: - Discontinue use of the lots of reagent listed above. - Review your historical quality control to ensure that the assay performance of these lots has been within your laboratory specifications. NOTE: Out-of-range high quality control results may indicate invalid test results. Consignees were asked to share this information with their laboratory staff and retain this notification as part of their laboratory Quality System documentation; and complete and return the enclosed response form within 10 days so that Beckman can be assured that they received this important notification. Assistance or questions regarding this notification, were directed to Technical Support at 1-800-854-3633 in the United States and Canada. Outside the United States and Canada, contact consignees were told to contact their local Beckman Coulter Representative.

Details

Recall number
Z-2178-2011
Initiated
December 17, 2009
Posted by FDA
May 10, 2011
Terminated
March 29, 2012
Product code
JIT – Calibrator, Secondary
Quantity
2,320 kits
Distribution
Distribution Nationwide and Canada.
Recalling firm
Beckman Coulter Inc., Brea, CA

Official FDA recall record