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Invuity, Inc. recalls INVUITY(R) PhotonBlade(TM), REF PB1
Recalled August 2, 2017 · FDA recall Z-2778-2017 · Invuity
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. · FDA Class II
Units
1328 units
Sold at
nationwide
Description
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.
Product
INVUITY(R) PhotonBlade(TM), REF PB1
Manufacturer(s)
Invuity, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →