Data Foundry

Medical device recalls 2013

FLEXSTENT Femoropopliteal Self-Expanding Stent System — Class II medical device recall Z-1511-2013

Terminated recall by Cordis Corporation, reported 2013-06-12, distributed nationwide. Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under some conditions, and to a lesser degr

Recall numberZ-1511-2013
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmCordis Corporation, Miami Lakes, FL, United States
Recall initiated2013-04-23
Classified2013-06-06
Reported by FDA2013-06-12
Terminated2014-06-27
DistributedNationwide (US)
Countries outside the USCZ, IT, NL, NZ
Quantity310 units
Model numbersFLX-50030-V2, FLX-50040-V2, FLX-50060-V2, FLX-50080-V2, FLX-50100-V2, FLX-50120-V2, FLX-50150-V2, FLX-50200-V2, FLX-60030-V2, FLX-60040-V2, FLX-60060-V2, FLX-60080-V2, FLX-60100-V2, FLX-60120-V2, FLX-60150-V2, FLX-60200-V2, FLX-70030-V2, FLX-70040-V2, FLX-70060-V2, FLX-70080-V2, FLX-70100-V2, FLX-70120-V2, FLX-70150-V2, FLX-70200-V2, FLX-80030-V2 and 7 more

Product

FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT¿ Femoropopliteal SES clinical product is indicated for treatment of atherosclerotic de novo native superficial femoral artery lesions and proximal popliteal lesions.

Reason for recall

Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under some conditions, and to a lesser degree, in the outer pouch.

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-1511-2013. 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.