Covidien Valleylab FT10 — Class II medical device recall Z-0631-2024
Ongoing recall by Covidien, reported 2024-01-10, distributed nationwide. Due to software issue, New systems may exhibit an error which may prohibit use of new systems resulting in sys
| Recall number | Z-0631-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien, Lafayette, CO, United States |
| Recall initiated | 2023-11-16 |
| Classified | 2024-01-03 |
| Reported by FDA | 2024-01-10 |
| Distributed | Nationwide (US) |
| Quantity | 47,901 units |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 10884521516328, 10884521640474, 10884521787056 |
| Model numbers | DLVLFT10GEN, VLFT10GEN, VLFT10GENZD |
Product
Covidien Valleylab FT10, FT Series Energy Platform, REF: VLFT10GEN, DLVLFT10GEN, VLFT10GENZD
Reason for recall
Due to software issue, New systems may exhibit an error which may prohibit use of new systems resulting in system being inoperable
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-0631-2024. 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.