Medical device adverse event reports are often incomplete, inaccurate and delayed
2 sources·Updated October 15, 2026
Covered by 2 sources
- News-Medical·4h agoBulk adverse event reporting may delay medical device safety warnings
Permitting medical device manufacturers to submit bulk summary reports of adverse events to the US Food and Drug Administration (FDA), rather than reporting individual cases, often fails to promptly detect potential safety signals, finds a study published by The BMJ today.
Read at News-Medical → - Medical Xpress·8h agoMedical device adverse event reports are often incomplete, inaccurate and delayed
Permitting medical device manufacturers to submit bulk summary reports of adverse events to the U.S. Food and Drug Administration (FDA), rather than reporting individual cases, often fails to promptly detect potential safety signals, finds a study published by The BMJ. This is a…
Read at Medical Xpress →
