FDA Device recall Z-2778-2017
INVUITY(R) PhotonBlade(TM), REF PB1
- FDA Device
- Class II
- terminated
- Published 2017-08-02
On 2017-08-02 the FDA classified a Class II recall of INVUITY(R) PhotonBlade(TM), REF PB1 by Invuity, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2778-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-12 |
| Published | 2017-08-02 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Invuity |
| Distribution | US |
Product
INVUITY(R) PhotonBlade(TM), REF PB1
Reason
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.
Identifiers
| code_info | All Lot Numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2778-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.