Covidien LLC recalls Biosyn Monofilament Absorbable Suture 6/0 30" VIOLET CV-23, Item Code UM201
- Recall date
- December 18, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1300-2020
- FDA classification
- Class II
- Brand / firm
- Covidien LLC
- Sold / distributed
- US Nationwide distribution.
Why it was recalled
There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Biosyn Monofilament Absorbable Suture 6/0 30" VIOLET CV-23, Item Code UM201
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