Covidien Force TriVerse electrosurgical device 10 cord-Intended as… — Class II medical device recall Z-1020-2019
Terminated recall by Covidien, PLC, reported 2019-03-27, distributed nationwide. Potential for the sterile packaging to be compromised
| Recall number | Z-1020-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien, PLC, Boulder, CO, United States |
| Recall initiated | 2019-02-15 |
| Classified | 2019-03-18 |
| Reported by FDA | 2019-03-27 |
| Terminated | 2020-06-17 |
| Distributed | Nationwide (US) |
| Quantity | 850 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10884524000084, 20884524000081 |
| Lot numbers | 80390309X |
| Model numbers | FT3000F |
Product
Covidien Force TriVerse electrosurgical device 10 cord-Intended as electrosurgical energy to cut and/or coagulate tissue. Product Usage: Single-use device intended for use in open procedures (such as general, urologic, thoracic, plastic and reconstructive, gynecologic) and minimally invasive arthroscopic procedures where the surgeon desires monopolar radio-frequency electrosurgical energy to cut and/or coagulate tissue. The electrosurgical device is intended for use with conventional monopolar electrosurgical electrodes. Item Code: FT3000F
Reason for recall
Potential for the sterile packaging to be compromised
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-1020-2019. 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.