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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
InitiatedRecall #ClassStatusReasonQuantityLink basis
2022-05-25Z-1806-2022Class IIIOpen, ClassifiedFacility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21. This device with this specific storage temperature deviation is not likely to cause adverse health consequences.Distribution: US Nationwide distribution.a. .03bx b. 204bx c. 34bxcode info di
Regulatory clearances

    Predicate lineage

    Cited as predicate by: K210718, K210974

    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
    2016-03-03NAINo action indicatedMcKesson Medical-Surgical Inc0
    2012-05-01NAINo action indicatedMcKesson Medical-Surgical Inc.0
    2011-12-08NAINo action indicatedMcKesson Medical-Surgical2
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