FDA Enforcement Class II Terminated

Integra Hallu-Fix cannulated screw driver (model number P/N 129733ND) and cannulated screwdriver tip (model number P/N 129735ND). Indicated for use in fixation of fractures, osteotomies and arthrodesis of the first metatarso-phalangeal joint.

Recall: Z-1685-2013 · Reported July 17, 2013

Enforcement

Recall Number
Z-1685-2013
Event ID
65503
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Integra LifeSciences Corp.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Report Date
July 17, 2013
Initiation Date
February 1, 2013
Classification Date
July 11, 2013
Termination Date
July 25, 2013
Address
311 Enterprise Dr, N/A, Plainsboro, NJ, 08536-3344, United States

Description

Integra Hallu-Fix cannulated screw driver (model number P/N 129733ND) and cannulated screwdriver tip (model number P/N 129735ND). Indicated for use in fixation of fractures, osteotomies and arthrodesis of the first metatarso-phalangeal joint.

Reason

The firm has received numerous complaints of the cannulated screw driver tip breaking during surgery.

Code Info

The following lots of the cannulated screw driver (model number P/N 129733ND) were affected: D2ZG, D32L, D3HV, D3PG and E0U3. The following lots of the cannulated screwdriver tip (model number P/N 129735ND) were affected: D2ZQ and D3EC.

Distribution

Worldwide Distribution-USA (nationwide) including the states of AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, MI, MN, MO, MT, NC, NE, NJ, NV, NY, OH, PA, RI, SC, TN, TX, UT, VA, and WA and the countries of Canada, Austria, Belgium, Switzerland, Czech Republic, Germany, Denmark, Spain, Finland, France, Ireland, Israel, Italy, Lebanon, Luxembourg, Netherlands, Norway, Portugal, Russia, Saudi Arabia, Sweden, United Arab Republic, United Kingdom, and South Africa.

Quantity

154 screwdrivers were distributed; 67 screwdriver tips were distributed.