ClearanceBrief
Recall Z-0879-2009 ยท HTZ Instrument, Cutting, Orthopedic

Biomet, Inc.

Biomet Microplasty Elite Instruments Vanguard Slidex Femoral Block, 70 mm, Biomet Orthopedics, Inc., Warsaw, IN; REF 32-485156. A manual surgical instrument for general use; a non-powered, hand-held, or hand-manipulated device; instrument guide.

DateJan 13, 2009 (initiated Dec 18, 2008)
StatusTerminated
ReasonFalling component: The universal pin, which holds the sliding instrument saw guide in its slot, may loosen during surgical procedures and fall into the wound.
Root causeOther
ActionConsignees were notified by letter entitled "URGENT MEDICAL DEVICE REMOVAL NOTICE" dated 12/18/08 advising them of the problem and that the instruments should be removed from use and returned. For further information, please contact Biomet, Inc., by telephone on 800-348-9500.
Quantity444 of all products
DistributionWorldwide Distribution --- including USA and countries of Australia, Canada, Japan and the United Kingdom.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.