Centurion Medical Products product recalled over sterility concerns
- Recall date
- March 9, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Centurion Medical Products Corporation recalls POST-OP EYE TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they a…
- Recall number
- Z-1730-2017
- FDA classification
- Class II
- Brand / firm
- Centurion Medical Products Corporation
- Sold / distributed
- US Distribution: NY, NC, PA, CA, OH, WA, VA, NJ, IL
Why it was recalled
Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential breach in sterile packaging.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
POST-OP EYE TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
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