FDA Recall Terminated

Inhibin A ELISA, Part Number: DSL-10-28100-4 Product Usage: The Inhibin A ELISA kit is intended for the quantitative measurement of dimeric Inhibin A in human serum or plasma. It is intended strictly for in vitro use as an aid in the diagnosis and monitoring of various hormonal reproductive disorders.

Recall: Z-3128-2011 · Initiated November 10, 2010

Recall

Recall Number
Z-3128-2011
Event Number
59685
Firm
Beckman Coulter Inc.
FEI Number
2050012
Product Code
NDR
Status
Terminated
Root Cause
Other
Initiated
November 10, 2010
Posted
September 2, 2011
Terminated
July 11, 2012
Address
250 S Kraemer Blvd, Brea, CA, 92821-6232

Description

Inhibin A ELISA, Part Number: DSL-10-28100-4 Product Usage: The Inhibin A ELISA kit is intended for the quantitative measurement of dimeric Inhibin A in human serum or plasma. It is intended strictly for in vitro use as an aid in the diagnosis and monitoring of various hormonal reproductive disorders.

Reason

The recall was initiated because Beckman Coulter has confirmed the microbial contamination in the conjugate diluent bottles included in the Manual Inhibin A Elisa kit (Part Number DSL-10-28100-4), kit lot number 110761.

Action

Beckman Coulter initiated an "URGENT PRODUCT CORRECTION" on June 15, 2011, via a telephone script to the only one customer impacted by the recalled product. The telephone script provided an explanation of the problem identified and the actions to be taken. Beckman Coulter recommended that the customer discontinue use of the recalled product as a preventative measure. Beckman will send a representative to the customer's facility to replace the recalled product in all remaining kits of the affected lot. The customer was instructed to share this information with laboratory staff. For any questions concerning this information, contact Beckman Coulter at 952-368-7874.

Distribution

(USA) Nationwide Distribution in the state of CA

Quantity

342 units