Lifecore Biomedical, Inc.
FDA adverse event reports naming Lifecore Biomedical, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: LIFECORE BIOMEDICAL, INC..
- Total reports
- 1,804
- Deaths
- 3
- Injuries
- 1,740
- Malfunctions
- 17
Reports per year
Source: FDA adverse event reports by year received, 1996–2014. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
- 2004-07-20TerminatedOther
TefGen is an implant material which is intended to be used as a temporary space-making barrier over bone or other tissue.
Packaged product labeled catalog #TFS30, lot number 002419 actually contained catalog #TFR60, lot number 002441and vice versa.
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