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Medline

MEDLINE INDUSTRIES, INC. · Model MDS200100 · UDI-DI 30080196729580

LRT
5
510(k) clearances
10
Adverse events
1
Recalls
2
Facilities

Description

STRIP,STEAM INDICATOR,4"

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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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.