FDA Device recall Z-1472-2014
Fassier-Duval IM Telescopic System
- FDA Device
- Class II
- terminated
- Published 2014-04-30
On 2014-04-30 the FDA classified a Class II recall of Fassier-Duval IM Telescopic System by Pega Medical, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1472-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-03-05 |
| Published | 2014-04-30 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Pega Medical |
| Distribution | US |
Product
Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant. Catalogue number FD-040(L)-SS. -Duval IM Telescopic System.
Reason
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.
Identifiers
| code_info | Catalogue Number: FD-040(L)-SS Lot #: 111208-03 and 110808-13 111019-01 and 110808-13 110302-01 and 110808-13 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1472-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.