FDANovember 12, 2020device
Stimulan Kit 10cc, Model 600-010 - Product Usage: intended for use as a bone void filler for voids or gaps that are not intrinsic to the stability of the bony structure.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The product is mislabeled.
What to do
FDA enforcement status: Terminated
Brands named
biocomposites
Recall history
No related federal recalls on record for this brand yet.
Own something like this?
AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.
Start free — 200 items, no card →