FDA Recall Terminated

Compress Short Anchor Plug Holder, 13mm, Biomet Orthopedics, Inc., Warsaw, IN; REF CP461038. Non-powered, hand-held device intended for medical purposes for use with other devices in orthopedic surgery.

Recall: Z-0521-2009 · Initiated July 18, 2008

Recall

Recall Number
Z-0521-2009
Event Number
49014
Firm
Biomet, Inc.
FEI Number
1825034
Product Code
LXH
Status
Terminated
Root Cause
Process control
Initiated
July 18, 2008
Posted
January 7, 2009
Terminated
July 7, 2009
Address
56 E Bell Dr, Warsaw, IN, 46581-0587

Description

Compress Short Anchor Plug Holder, 13mm, Biomet Orthopedics, Inc., Warsaw, IN; REF CP461038. Non-powered, hand-held device intended for medical purposes for use with other devices in orthopedic surgery.

Reason

The set screw may not fully seat, which will prevent the handle from mating to the instrument during use.

Action

Distributors were notified via an Urgent Medical Device Removal Notice, dated 7/18/08, which instructed them to locate and remove the instruments, carefully follow the instructions on the enclosed "FAX Back Response Form," fax a copy of the Response Form to 574-372-1683 prior to return of product, and to notify the hospital personnel via a copy of a recall letter. The letter also stated that the instruments would be reworked and returned to the distributors. Distributors are to confirm receipt of the notice by calling, 800-348-9500, ext 3983. Questions related to the notice should be directed to Mary Hardesty at 800-348-9500 or 574-372-3983.

Distribution

Worldwide Distribution --- including USA and countries of Australia, Belgium and Finland.

Quantity

41 of all products.