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Adverse-event reports (MAUDE)

Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.

No adverse-event reports are linked to this device.

Recall history

No recalls linked.

Regulatory clearances

    Predicate lineage

    Cited as predicate by: K150134, K170329, K260892

    Cited as predicate by: K153633, K221676

    Lineage each submission cites, walked transitively (indented = the cited device's own predicates). Extracted from public 510(k) summary text — heuristic, and includes reference devices mentioned alongside true predicates.

    Manufacturer compliance record
    DateTypeOutcomeFacilityCitations
    2014-08-27NAINo action indicatedMedela Inc0
    2014-08-27NAINo action indicatedMedela Inc0
    2014-02-26NAINo action indicatedMedela Inc0
    2014-02-26NAINo action indicatedMedela Inc0
    2012-05-25OAIOfficial action indicatedMedela Inc7
    2012-05-25OAIOfficial action indicatedMedela Inc7
    2011-11-21NAINo action indicatedMedela Inc0
    2011-11-21NAINo action indicatedMedela Inc0
    2011-08-09VAIVoluntary action indicatedMedela Inc0
    2011-08-09VAIVoluntary action indicatedMedela Inc0
    2011-02-25WLWarning LetterMedela Inc—
    2011-02-25WLWarning LetterMedela Inc—
    2010-11-01OAIOfficial action indicatedMedela Inc0
    2010-11-01OAIOfficial action indicatedMedela Inc0
    2010-01-21VAIVoluntary action indicatedMedela Inc7
    2010-01-21VAIVoluntary action indicatedMedela Inc7
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