ClearanceBrief
Recall Z-0375-2010 ยท HSB Rod, Fixation, Intramedullary And Accessories

Zimmer Inc.

Zimmer Natural Nail System, Antegrade Femoral Targeting Guide Handle, standard, nonsterile, Zimmer, Warsaw, IN; REF 00-2490-001-00. The device is used to drill into the proximal tibia or distal femur for placement of screws that stabilize the position of an intramedullary nail implant. The targeting guide instrumentation serves to assist the surgeon in precisely drilling into the bone and through

DateNov 24, 2009 (initiated Jul 1, 2009)
StatusTerminated
ReasonThe guides may come apart during use, some guides may experience surface cracking, guide handles and modules may not target the femoral nail holes accurately and the instruments may not be able to be assemble together due to a change in the threading method used.
Root causeOther
ActionOn July 1, 2009, U.S. distributors were notified by e-mail to return two instruments. The recall was expanded with international accounts notified by e-mail on August 5, 2009, and U.S. accounts being notified by e-mail on August 6, 2009, to return 7 instruments. The scope of the recall was then expanded again to include 14 instruments and another letter dated September 14, 2009 to distributors and user accounts. The notifications described the affected products, problem, health risks and actions for consignees. Direct questions about the recall to Zimmer, Inc. by calling 1-800-613-6131.
Quantity327 of total product
DistributionWorldwide Distribution -- United States, France, Germany, Italy, Switzerland and United Kingdom.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K082770ZIMMER NATURAL NAIL SYSTEM TIBIAL NAIL
Zimmer, Inc., Dec 11, 2008
K083497ZIMMER NATURAL NAIL SYSTEM PIRIFORMIS FOSSA AND GREATER TROCHANTER ANTEGRADE FEMORAL NAILS
Zimmer, Inc., Feb 19, 2009
K090596ZIMMER NATURAL NAIL SYSTEM STAINLESS STEEL TIBIAL NAIL & STAINLESS PIRIFORMIS FOSSA AND GREATER TROCHANTER ANTEGRADE FEM
Zimmer, Inc., Jun 30, 2009