FDA Enforcement Class II Terminated

TI Single Vector Distractor Body with Right Foot/20mm; Catalog ID 487.962 The Titanium Single Vector Distractor and Proximal Foot Plates are intended for mandibular bone lengthening where gradual bone distraction is required, including conditions such as congenital mandibular deficiencies or post-traumatic defects.

Recall: Z-2581-2016 · Reported August 24, 2016

Enforcement

Recall Number
Z-2581-2016
Event ID
74419
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Synthes (USA) Products LLC
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
August 24, 2016
Initiation Date
May 23, 2016
Classification Date
August 17, 2016
Termination Date
December 13, 2016
Address
1301 Goshen Pkwy, N/A, West Chester, PA, 19380-5986, United States

Description

TI Single Vector Distractor Body with Right Foot/20mm; Catalog ID 487.962 The Titanium Single Vector Distractor and Proximal Foot Plates are intended for mandibular bone lengthening where gradual bone distraction is required, including conditions such as congenital mandibular deficiencies or post-traumatic defects.

Reason

DePuy Synthes is voluntarily initiating a recall due to a possibility the fastener on the Titanium Single Vector Distractor Body may become prematurely separated from the Proximal Foot Plate.

Code Info

Part # 487.962, Lot # A4JY080; 4042146; 4042147; 4365410; 4548558; 4664392; 5041113; 5041114; 5041162; 5071337; 5229307; 5414447; 5414448; 5414449; 5422905; 5621082; 5621083; 5621088; 5696010; 6164423; 6164425; 6164555; 6171239; 6171240; 6397761; 7537258; 7927945, mfg date 09JUN1999 -30JUN2015, exp date 22MAR2020-30JUN2035

Distribution

Worldwide Distribution-US (nationwide) distribution to states of: AZ, CA, CO, DC, FL, IL, MA, MI, NJ, NY, PA, TX, UT, WI, and WV; and countries of: Australia, Canada and Switzerland.

Quantity

90 units