ClearanceBrief
Recall Z-0906-2014 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Exactech, Inc.

***REF 186-01-08***InteGrip ACETABULAR AUGMENT***SMALL 8mm. Use with 48/50mm Shell.***EXACTECH, Gainesville, FL 32653-1630. The Exactech Novation InteGrip Acetabular Augments are indicated for use in skeletally mature individuals undergoing primary or revision surgery for hip replacement and whose orthopedic surgeon desires a prosthetic alternative to structural allograft in cases of segmental ac

DateFeb 3, 2014 (initiated Sep 11, 2013)
StatusTerminated
ReasonExactech is recalling the InteGrip Acetabular Augments due to an out of range condition for an in-vitro biological evaluation standard.
Root causeEmployee error
ActionExactech sent an "Important Product Recall Notice" dated September 11, 2013, to all affected customers. The letter identified the product and the action needed to be taken by the customers. Customers were instructed to cease distribution or use of the products. Extend this information to your accounts that may have this product in their possession. Verify if you have any of the subject InteGrip Acetabular Augments (catalog numbers 186-01-08 to 186-05-13) in the specified lots. Complete and fax back the attached form. Further questions, please call 1-800-392-2832.
Quantity235
DistributionUSA Distribution including the states of : FL, VA, NY, OH, ME, TX, CO, and GA.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K101761EXACTECH NOVATION EMPIRE ACETABULAR AUGMENT WITH INTEGRIP MODEL 186-01-08/11/13, 186-02-08/11/13, 186-03-08/11/13
Exactech, Inc., Sep 21, 2010
K113609NOVATION INTEGRIP ACETABULAR AUGMENTS, GROUPS 4 AND 5
Exactech, Inc., Jan 4, 2012