ClearanceBrief
Recall Z-1494-2011 ยท HSB Rod, Fixation, Intramedullary And Accessories

Pega Medical Inc.

Male Driver 4.0mm (catalog # MDr140L) and Male Driver 3.2mm (catalog # MDr132L), an instrument used for the insertion of the Fassier-Duval Telescopic IM System intramedullary nail, for bone fixation.

DateMar 2, 2011 (initiated Jan 29, 2010)
StatusTerminated
ReasonPossible breakage. Structural weakness has been detected on the Male Driver 3.2mm and 4.0mm sizes. In certain cases, this weakness could lead to a premature failure of the instrument if it is submitted to large torsional loads higher than the normal forces required to introduce the male component.
Root causeProcess control
ActionOn 01/29/2010, Pega Medical began contacting their consignees by e-mail and telephone. Pega Medical followed up with their consignees by sending out the replacement components along with the explanation letter. The subject on the letter is Notice for 3.2 mm and 4.0 mm Male Drivers of the Fassier-Duval IM Telescopic System. The consignees were informed that there could be a structural weakness in some of the Male Driver instruments. This problem has been detected on the 3.2mm and 4.0mm sizes. In certain cases, this weakness could lead to a premature failure of the instrument if it is submitt
Quantity4 units of MDr132L (3.2 mm) and 3 units of MDr140 (4.0 mm) distributed in US.
DistributionComponents were distributed to four hospitals in the US in the state of GA, OK, TN, and UT.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K020885FASSIRE-DUVAL TELESCOPIC IM SYSTEM
Pega Medical, Inc., Feb 6, 2003
K041393FASSIER-DUVAL TELSCOPIC IM SYSTEM
Pega Medical, Inc., Aug 17, 2004