Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments — Class II medical device recall Z-1867-2016
Terminated recall by Integra LifeSciences Corp., reported 2016-06-08, distributed in AR, CA, CO, FL, IN, KY, MA, MI…. Reports relating to unintended patient or operator burns or operator electric shock for some of Integra's Micr
| Recall number | Z-1867-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Integra LifeSciences Corp., Plainsboro, NJ, United States |
| Recall initiated | 2016-03-07 |
| Classified | 2016-05-31 |
| Reported by FDA | 2016-06-08 |
| Terminated | 2017-03-31 |
| Distributed | AR, CA, CO, FL, IN, KY, MA, MI, NC, NJ, NM, NY, OH, TN, TX, WA, WI |
| Quantity | 2,487 instruments |
| Model numbers | CEV669E |
Product
Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments
Reason for recall
Reports relating to unintended patient or operator burns or operator electric shock for some of Integra's MicroFrance electrosurgical instruments.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1867-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.