FDA Enforcement Class II Terminated

Accell Evo3C Demineralized Bone Matrix, 5 cc, Model Number: 02-6000-050 , Lot Number: 132160. Product Usage: Accell Evo3c Demineralized Bone Matrix Putty is intended for filling voids and gaps in the skeletal system that are not intrinsic to the stability of the bony structure. Accell Evo3c is indicated for use as a bone graft extender in the spine, extremities and pelvis, or as a bone void filler in the extremities and pelvis. The voids or gaps may be surgically created defects or the result of traumatic injury to the bone.

Recall: Z-1868-2014 · Reported July 2, 2014

Enforcement

Recall Number
Z-1868-2014
Event ID
68330
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Integra LifeSciences Corp.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
July 2, 2014
Initiation Date
May 19, 2014
Classification Date
June 24, 2014
Termination Date
September 5, 2014
Address
311 Enterprise Dr, N/A, Plainsboro, NJ, 08536-3344, United States

Description

Accell Evo3C Demineralized Bone Matrix, 5 cc, Model Number: 02-6000-050 , Lot Number: 132160. Product Usage: Accell Evo3c Demineralized Bone Matrix Putty is intended for filling voids and gaps in the skeletal system that are not intrinsic to the stability of the bony structure. Accell Evo3c is indicated for use as a bone graft extender in the spine, extremities and pelvis, or as a bone void filler in the extremities and pelvis. The voids or gaps may be surgically created defects or the result of traumatic injury to the bone.

Reason

This lot of Accell Evo3C Demineralized Bone Matrix, 5cc was incorrectly packaged in boxes that describe the product as Accell Evo3 Demineralized Bone Matrix. Evo3C is contraindicated for treatment of vertebral compression and not indicated for use in the posterolateral spine.

Code Info

Model Number: 02-6000-050 , Lot Number: 132160.

Distribution

US Nationwide Distribution

Quantity

61