RecallDepth

Slipped Capital Femoral Epiphysis System Product Usage: Intended for fracture fixation of large bones and large bone fragments and for slipped capital femoral epiphysis, pediatric femoral neck fractures, intercondylar femur fractures and sacroiliac joint disruptions.

Company
Synthes Usa (Hq), Inc.
Recall Initiated
July 31, 2013
Posted
November 27, 2013
Terminated
June 1, 2015
Recall Number
Z-0408-2014
Quantity
166
Firm Location
West Chester, PA

Reason for Recall

There is a possibility for the Guide Wires of the Slipped Capital Femoral Epiphysis System to stick in the cannulation of the drill bit and the drill bits to break during surgery.

Distribution

USA Nationwide Distribution

Lot / Code Info

Parts 03.207.001 and 03.207.008 with lot numbers:   Part # Lot # 03.207.001 PE00376  PE00439  PE01391  PE01329  PE01412  PE00504 03.207.008 PE00440  PE00377  PE00513  PE01475  PE01691

Root Cause

Device Design

Action Taken

Synthes sent an Urgent Notice: Medical Device Recall letter dated July 30, 2013 to all affected customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to review their inventory, immediately remove the affected product and return to Credit/Returns, Synthes. For questions call 610-719-5450.

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