Recall StatusTerminated
Date Initiated2015-04-10
Date Terminated2015-07-10
Product Quantity(244 units in US and 61 units OUS)
Reason for Recall
During a field audit it was discovered by an employee that a 16mm Trestle Luxe Screw has been both laser marked and labeled as a 14mm Trestle Luxe Screw (4.0mm Variable Angle, Self-Drilling Hexalobe Screw, 14mm). As a result the firm recalling the affected lots codes for this mislabeling.
Firm Action
Alphatec Spine sent an Urgent-Medical Device Recall Notification dated April 7, 2015, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. The firm first requested that customers notify their consignees of the recall and the risk, and risk mitigation factors.
The firm requests that customers take the following field actions:
-Upon receipt of the Field Safety Notice to review inventory to determine if affected screw --part number 71240-14, lot 685904 is in their possession.
-If the product is in their possession to please abstain from use and contact Alphatec Spine Customer Service (
[email protected]) immediately for instructions on how to return the affected product. All shipping instructions will be provided, including replace product and/or credit.
-Fill out page 3 of the letter to confirm that they have read the notification and have take all necessary actions stated in the notification.
-Return a signed copy using one of the methods below:
Mail to: Alphatec Spine, Inc.
5818 El Camino Real
Carlsbad, CA 92008
Fax to: 1-800 431-7729 For further questions call ( 760) 431-9286.
Distribution Pattern
Worldwide Distribution - US Distribution to the states of: KS, LA, TN, NJ, KY, CA, FL, OR, OK, AZ, WI, CO, IN, NH, AR, UT, and AL., and to the countries of : Spain, Japan, Belgium, and Saudi Arabia.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.