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Indicator, Sterilization

FDA product code LRT · Class 2 · General Hospital

22
Registered devices
10
Adverse events
1
Recalls
5
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2012-08-02Steris CorporationOn 7/20/2012 the firm became aware that a lot of tubing was distributed by the supplier after it was rejected by Steris due to failing process indicators.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.