Covidien Force TriVerse Electrosurgical Devices — Class II medical device recall Z-1446-2020
Terminated recall by Covidien Llc, reported 2020-03-11, distributed nationwide. Sterile packaging may potentially be compromised, and use of products may result in increased risk for infecti
| Recall number | Z-1446-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien Llc, Mansfield, MA, United States |
| Recall initiated | 2020-02-10 |
| Classified | 2020-03-05 |
| Reported by FDA | 2020-03-11 |
| Terminated | 2024-04-26 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, CA, CH, CZ, DE, DK, ES, FI, FR, GB, GR, HU, IT, JO, KE, LT, LU, PL, PT, RO, RS, SE, SK |
| Quantity | 70,361 |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10884524000084, 10884524001937, 20884524000081, 20884524001934 |
| Lot numbers | 181170378R, 181170379R, 181170380R, 190530412R, 190530413R, 190600130R, 190630011R, 190640010R, 190880338R, 190880339R, 190880340R, 190880341R, 191020334R, 191090309R, 191090310R, 191160340R, 191160341R, 191160342R, 191300316R, 191300317R, 191370322R, 191370323R, 191440286R, 191440287R, 191510192R, 191510193R, 191580245R, 191580246R, 191580247R, 191650217R, 191650218R, 191650219R, 191720259R, 191720261R, 191790222R, 191790223R, 191790224R, 191860195R, 191860197R, 191860198R and 40 more |
Product
Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084 20884524000081; 10884524001937 20884524001934
Reason for recall
Sterile packaging may potentially be compromised, and use of products may result in increased risk for infection.
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-1446-2020. 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.