Skip to the content

FDA Medical Device Recalls (openFDA)

Encore Medical, Lp: 3DKNEE SYSTEM, 3D Knee Tibial Insert-DCM, Sterile, Right, size 4 x 11mm. Encore Medical, LP. Austin, TX 78758-5445. Intended to aid the surgion in relieving the patient of knee pain and restoring knee joint function.

Recall number
Z-1433-2010
Recalling firm
Encore Medical, Lp
Product
3DKNEE SYSTEM, 3D Knee Tibial Insert-DCM, Sterile, Right, size 4 x 11mm. Encore Medical, LP. Austin, TX 78758-5445. Intended to aid the surgion in relieving the patient of knee pain and restoring knee joint function.
Status
Terminated
Initiated
2010-03-19
Posted
2010-04-26
Terminated
2010-07-22
Reason
Affected product had incorrect color label which is a secondary visual indicator for sizing.
Root cause
Packaging process control
Action
Encore Medical, LP notified consignees by e-mail dated March 19, 2010. Consignees were requested to return the affected product to the firm. For further information, contact Encore Medical, LP at 1-888-838-3668.
Quantity
7 units
Distribution
Worldwide Distribution -- United States (UT, IA) and Germany.
Lot, serial or model codes
Catalog Number: 392-11-604, Lot Number: 59600085.
510(k) numbers
["K020114"]
PMA numbers
not on file
Product code
JWH
Firm FEI
1000116912
Firm city
Austin
Firm state
TX
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

Search this register