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Terminated

Ratcheting Torque Limiting Handle, Catalog Number 52-1012, Orthofix Spinal Implants, Firebird Spinal Fixation System, Firebird Spinal Fixation System DDD Instrument Case. Product is intended for use with the Set Screw Driver (52-1061) and Adjustable Counter Torque Wrench (52-1265) to perform the final tightening of set screws in a spinal implant construct.

FDA Recall Z-3162-2011 · Posted 2011-09-07

Recalling FirmOrthofix, Inc.
Recall StatusTerminated
Product CodeNKB
Date Initiated2011-04-01
Date Terminated2012-03-23
Product Quantity287 units

Reason for Recall

Upon reaching torque limit, there is a possibility the product may jam or exhibit a ratchet direction switch from forward to reverse.

Firm Action

Orthofix, Inc. sent an "URGENT PRODUCT RECALL NOTIFICATION" letter dated April 1, 2011 to all affected customers. The letter describes the product, problem, and the actions to be taken by the customers. The letter instructs customers to identify and remove the affected product from use. Customers were advised to use the combination of the Ratching R Handle and the Set Screw Driver if they experience problems with the Ratching Torque Limiting Handle. A Tracking and Verification form was attached for customers to complete and return to the Orthofix Inc. Regulatory Affairs Department via fax at 214-937-3322. Contact your Account Services Representative at 888-298-5700 for questions regarding the removal and return of the affected product.

Root Cause

Device Design

Distribution Pattern

Worldwide Distribution-USA (nationwide) and Puerto Rico and the countries of Australia and Germany.

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.

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