Fassier-Duval IM Telescopic System — Class II medical device recall Z-1472-2014
Terminated recall by Pega Medical Inc., reported 2014-04-30, distributed nationwide. The outer package label contained the incorrect length of the device. There is a label on the outer package an
| Recall number | Z-1472-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pega Medical Inc., Laval, N/A, Canada |
| Recall initiated | 2014-03-05 |
| Classified | 2014-04-18 |
| Reported by FDA | 2014-04-30 |
| Terminated | 2014-05-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, CA, CO, DE, DK, ES, FR, GB, GR, IL, LT, MX, PE, SG |
| Quantity | 48 |
| Reason classes | labeling |
| Lot numbers | 110302-01, 110808-13, 111019-01, 111208-03 |
| Model numbers | FD-040 |
Product
Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant. Catalogue number FD-040(L)-SS. -Duval IM Telescopic System.
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1472-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.