FDA Device recall Z-1867-2016
Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments
- FDA Device
- Class II
- terminated
- Published 2016-06-08
On 2016-06-08 the FDA classified a Class II recall of Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments by Integra Lifesciences, citing reports relating to unintended patient or operator burns or operator electric shock for some of Integra's MicroFrance electrosurgical instruments.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1867-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-03-07 |
| Published | 2016-06-08 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Integra Lifesciences |
| Distribution | AR, CA, CO, FL, IN, KY, MA, MI, NC, NJ, NM, NY, OH, TN, TX, WA, WI |
Product
Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments
Reason
Reports relating to unintended patient or operator burns or operator electric shock for some of Integra's MicroFrance electrosurgical instruments.
Identifiers
| code_info | Catalogue No: CEV669E. All batch numbers distributed from January 2011 to February 17, 2016. |
|---|
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-1867-2016%22
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