Search Compliance About

MalfunctionGHM

MDR event

Received Apr 3, 2006

Report 2250051-2006-00140 · MDR key 695792

Device

Product problems

False Negative Result

Patient

Not reported

No Consequences Or Impact To Patient

inforMED sources data from the FDA's public MAUDE, recall, 510(k), and registration & listing databases via openFDA.

Not affiliated with the FDA. Data is unvalidated and may be incomplete — verify anything decision-critical against the source database.