ClearanceBrief
Recall Z-2371-2008 ยท GFA Blade, Saw, General & Plastic Surgery, Surgical

Biomet, Inc.

Exact Calcar Planer Rasp Style Blade, 42mm, Biomet Orthopedics, Inc, Warsaw, IN; REF 31-473796. Surgical blades used to remove excess bone proximal to the broach face to all instrument trial to seat properly.

DateSep 29, 2008 (initiated Jul 18, 2008)
StatusTerminated
ReasonThe blades will oxidize after the first cleaning.
Root causeProcess control
ActionDistributors were notified via letter dated 7/18/08 to locate and remove the products and to return them. Distributors were instructed to conduct the recall to the hospital level and to notify the hospitals of the recall by copy of an undated recall letter. Contact Biomet, Inc. at 1-800-348-9500, ext. 3983 for assistance.
Quantity141 of all products
DistributionNationwide and China.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.