Cordis Corporation recalls Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
- Recall date
- October 4, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0250-2020
- FDA classification
- Class II
- Brand / firm
- Cordis Corporation
- Sold / distributed
- US distribution to AL, AZ, FL, MN, and MO
Why it was recalled
Product was manufactured utilizing an expired inner body.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
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