FDA Recall Terminated

Captiva's lumbar intervertebral fusion system Reamers (color code rings on the Reamers).

Recall: Z-1480-2015 · Initiated February 25, 2015

Recall

Recall Number
Z-1480-2015
Event Number
70710
Firm
Captiva Spine, Inc 967 Alternate A1A Suite1
FEI Number
3006082533
Product Code
LXH
Status
Terminated
Root Cause
Device Design
Initiated
February 25, 2015
Posted
April 21, 2015
Terminated
June 1, 2015
Address
Jupiter, FL, 33477

Description

Captiva's lumbar intervertebral fusion system Reamers (color code rings on the Reamers).

Reason

It is possible for the titanium color-coded ring to detach from the Reamers.

Action

On 02/26/2015 the firm sent a Voluntary Correction Notification to its consignees via FedEx. Within that notification the firm asks to please check with your product representative and Central Supply Departments to determine if you have any of the products listed on the notificaiton. If any product is located please call 877-772-5571 from 8:30am (Eastern Time) to receive instructions as to how to remove the color-coded ring OR please follow the enclosed steps for the correction in their entirety. They contain information about returning the removed rings. Enclosed is Form 30.4 Product Tracking and Verification Form. You must complete and return this form even if you do not have any rings to remove and return. Please contact your Captiva Spine customer service representative if you have any questions regarding this correction, any of our products, or would like assistance with the correction.

Distribution

GA, IN, FL, UT, AZ, CA, and NY

Quantity

233 devices