FDAJune 12, 2017device
INVUITY(R) PhotonBlade(TM), REF PB1
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
A small number of customer observations were recently received which related to possible unintended energy discharge with the potential to cause tissue damage to patients.
What to do
FDA enforcement status: Terminated
Brands named
invuity
Recall history
No related federal recalls on record for this brand yet.
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