ClearanceBrief
Recall Z-2618-2017 ยท HWC Screw, Fixation, Bone

DePuy Mitek, Inc., a Johnson & Johnson Co.

DePuy Mitek LATARJET EXPERIENCE Top Hat Tap Product Code: 288203 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

DateMay 12, 2017
StatusTerminated
ReasonCombo Screw Driver (Product Code 288211) tip has the increased potential to break intra-operatively when being used at an angle off-axis to screw
Root causeComponent design/selection
ActionDePuy Mitek issued recall letter dated May 12, 2017 advising of the problem and requesting return of the product. A Response Form is to be completed and returned. Questions: contact your DePuy Synthes Mitek Sales Consultant or Carolyn Somerville, DePuy Mitek, Inc. (via telephone: 508.828.3647 Fax: 508.828.3762 or via email: DPYUS-MitekFieldActions@its.jnj.com).
Quantity153 units
DistributionUS: AZ, CA, CO, GA, MA, MI, OH, WA Foreign: Austria, Australia, Belgium, France, Germany, Spain, Switzerland, Netherlands, Poland, UK
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K083096LATARJET CORTICAL SCREW SET
Tag Medical Products, Apr 17, 2009
K091694MODIFICATION TO:LATARJET CORTICAL SCREW SET, MODELS 523JT, 523J (36-48MM)
Tag Medical Products, Jul 7, 2009
K110763LATARJET CORTICAL SCREW SET
T.A.G. Medical Products Corporation, Ltd., Apr 11, 2011