Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1812-2025 — PhenoMATRIX

U.S. FDA — Device Enforcement · Italy · 2025-05-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1812-2025
Date of alert
2025-05-06
Country / jurisdiction
Italy
Risk level
Class II
Risk type
recall
Brand
Copan WASP
Product category
device
Product type
Devices
Reported risk: AI-powered bacterial culture plate interpretation and workup software does not have Premarket Approval or pre-market notification (510(k)/de novo), so there is potential risk that the colony count and/or morphology information from images may not accurately reflect actual plate and may lead to inaccurate counts and/or morphology characteristics impacting patient diagnosis and subsequent care.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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