Philips Medizin Systeme Böblingen Gmbh
FDA adverse event reports naming Philips Medizin Systeme Böblingen Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH.
Total reports
5,826
Breakdown unavailable for this manufacturer. FDA filed these reports under a name containing characters the openFDA search API cannot match, so the death, injury and malfunction split, the yearly trend and the device categories can't be retrieved. The total above comes from openFDA's manufacturer index, which does return the name.
This is a limitation of the FDA's public API, not a gap in the underlying reports.
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