Stryker Sustainability Solutions recalls Launcher Guiding Catheter Model #LA6EBU30. Used in the coronary or peripheral vascular system..
- Recall date
- April 4, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1626-2016
- FDA classification
- Class II
- Brand / firm
- Stryker Sustainability Solutions
- Sold / distributed
- US distribution to KY.
Why it was recalled
Device packaging may not be sealed.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Launcher Guiding Catheter Model #LA6EBU30. Used in the coronary or peripheral vascular system..
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