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Recall Observatory FDA recall evidence

Device product

Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal, infra popliteal and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. The device is also indicated for post- dilatation of balloon-expandable and self-expanding stents in the peripheral vasculature.

Z-0998-2015

December 22, 2014

Class II

Product summary

Firm
Cordis Corporation
Event
Event 70080
Status
Terminated
Classification
Class II
Quantity
120
Official record key
device-enforcement:Z-0998-2015

Official wording

Reason: One unit from a demo lot of POWERFLEX PRO PTA Dilatation Catheter was left at a hospital and was not sterilized.

Code information: Catalog 4400615X, demo lot 15617883

Distribution pattern: Nationwide Distribution: US including states of: CT, NJ, NY, PA, MD, VA, WV, NC, SC, GA, FL, AL, TN, MS, KY, OH, IN, MI, IA, WI, SD, IL, MO, KS, NE, LA, OK, TX, CO, UT, AZ, CA, OR, WA, AR, IN, MN, WY, ND, NV, MA, RI, NH, CT, DE, District of Columbia and Hawaii.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    One unit from a demo lot of POWERFLEX PRO PTA Dilatation Catheter was left at a hospital and was not sterilized.