Pega Medical Inc.: Medical Device Recall in 2014 - (Recall #: Z-1472-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant. Catalogue number FD-040(L)-SS. -Duval IM Telescopic System.

Product Classification:

Class II

Date Initiated: March 5, 2014

Date Posted: April 30, 2014

Recall Number: Z-1472-2014

Event ID: 67803

Reason for Recall:

The outer package label contained the incorrect length of the device. There is a label on the outer package and an additional label on the product contained in the package.

Status: Terminated

Product Quantity: 48

Code Information:

Catalogue Number: FD-040(L)-SS Lot #: 111208-03 and 110808-13 111019-01 and 110808-13 110302-01 and 110808-13

Distribution Pattern:

Worldwide distribution, USA nationwide, Greece, United Arab Emirates, Peru, Canada, Israel, United Kingdom, France, Germany, Colombia, Mexico, Singapore, Lithuania, Denmark, and Spain.

Voluntary or Mandated:

Voluntary: Firm initiated