FDA Recall Terminated

NOVATION Femoral Stem, Tapered Extended offset, plasma- coated, press fit. Catalog number 160-01-13 intended to be implanted to replace a hip joint with our without bone cement.

Recall: Z-2086-2014 · Initiated March 7, 2014

Recall

Recall Number
Z-2086-2014
Event Number
68341
Firm
Exactech, Inc.
FEI Number
1038671
Product Code
LZO
Status
Terminated
Root Cause
Component design/selection
Initiated
March 7, 2014
Posted
July 21, 2014
Terminated
August 4, 2014
Address
2320 NW 66th Ct, Gainesville, FL, 32653-1630

Description

NOVATION Femoral Stem, Tapered Extended offset, plasma- coated, press fit. Catalog number 160-01-13 intended to be implanted to replace a hip joint with our without bone cement.

Reason

The femoral stem is lacking specified plasma coating.

Action

Exactech sent an Important Product Recall Notice dated March 10, 2014, to all affected customers. The notice identified the product the problem and the action to be taken by the customer. Description of Issue: The femoral stem is lacking specified plasma spray coating. Clinical Impact: Without plasma spray coating, the stem may not remain stable and will not have the possibility for biological fixation. In order to comply with applicable regulations and Exactech policies customers were instructed to : " Immediately cease distribution or use of these products. " Extend this information to your accounts that may have this product in their possession. " Determine if they have any of the affected devices " Fax back the attached form. Complete the attached fax back form and return it to Exactech. Customers were instructed to contact their Exactech inventory representative within 5 business days to confirm quantities at their location. For any inventory restocking questions related to this issue, please call 1-800-392-2832. For questions regarding this recall call 800-392-2832.

Distribution

Worldwide Distribution including Spain, Greece and Japan

Quantity

10