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Recall Observatory FDA recall evidence

Device product

Zilver 518 Vascular Self Expanding Stent The Zilver Vascular Stent is intended for use as an adjunct to percutaneous transluminal angioplasty (PTA) in the treatment of symptomatic disease of iliac arteries up to 100 mm in length with a reference vessel diameter of 5 to 9 mm. Patients should be suitable candidates for PTA and / or stent treatment.

Z-2309-2012

January 05, 2012

Class II

Product summary

Firm
Cook Ireland Ltd.
Event
Event 61451
Status
Terminated
Classification
Class II
Quantity
15 units of ZIV5-18-125-8-80 LOT# CF694429
Official record key
device-enforcement:Z-2309-2012

Official wording

Reason: Cook Ireland received a product complaint from Japan on December 22nd, 2011. The complainant reported that a 5 French Zilver Vascular Stent (part number ZIV5-18-125-8-80 from Lot# CF694429) was inserted into a sheath over a wire guide where it became lodged in the sheath hub. After further examination, the user determined that the product was a 6 French Zilver Vascular Stent (part number ZIV6-35

Code information: Part order number: ZIV5-18-125-8-80; Lot Number: CF694429; Expiration Date: 09-2014

Distribution pattern: Worldwide distribution: USA (nationwide) and country of: Japan.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Cook Ireland received a product complaint from Japan on December 22nd, 2011. The complainant reported that a 5 French Zilver Vascular Stent (part number ZIV5-18-125-8-80 from Lot# CF694429) was inserted into a sheath over a wire guide where it became lodged in the sheath hub. After further examination, the user determined that the product was a 6 French Zilver Vascular Stent (part number ZIV6-35