FDA Recall Terminated

Discovery Elbow System Humeral Condyle Set- Hexalobular, REF 114700, Lot 797550 Alloy, Sterile, Biomet Orthopedics Warsaw IN 46581. Intended for primary and revision joint arthroplasty for use in cemented applications.

Recall: Z-1071-2012 · Initiated December 14, 2011

Recall

Recall Number
Z-1071-2012
Event Number
60971
Firm
Biomet, Inc.
FEI Number
1825034
Product Code
JDC
Status
Terminated
Root Cause
Process change control
Initiated
December 14, 2011
Posted
February 21, 2012
Terminated
December 12, 2012
Address
56 E Bell Dr, Warsaw, IN, 46582-6989

Description

Discovery Elbow System Humeral Condyle Set- Hexalobular, REF 114700, Lot 797550 Alloy, Sterile, Biomet Orthopedics Warsaw IN 46581. Intended for primary and revision joint arthroplasty for use in cemented applications.

Reason

A Discovery Condyle Kit w/ Hexalobula was opened during an elbow joint replacement surgery, and was found to contain two male condyles.

Action

December 14, 2011 Urgent Medical Device Recall Notices were sent to Distributors and hospital OR managers describing the product, problem, risks associated with the recall, and actions to be taken. The notice included Instructions to locate and remove the product. Customers were asked to complete a response form and fax to 574-372-1683, prior to returning product by priority mail to the attention of Angi Dickson, Biomet , 56 East Bell Drive Warsaw, IN, USA 46580 with a copy of the response form. Receipt of the notice should also be confirmed by calling 800-348-9500, extension 3983 or 3009. Questions related to this notice should be directed to 574-371-3983 or 574-371-3009 Monday through Friday 8 AM to 5 PM.

Distribution

International Only Distribution -- Netherlands & UK.

Quantity

10 units