TLS2 Thermal Ligating Shears — Class II medical device recall Z-1698-2019
Terminated recall by Microline Surgical, Inc., reported 2019-06-12, distributed in ND, NY. The shears exhibited a high rate of complete or intermittent failure to actuate. As a result, they do not perf
| Recall number | Z-1698-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microline Surgical, Inc., Beverly, MA, United States |
| Recall initiated | 2019-03-22 |
| Classified | 2019-05-31 |
| Reported by FDA | 2019-06-12 |
| Terminated | 2020-07-30 |
| Distributed | ND, NY |
| Countries outside the US | DE, NL |
| Quantity | 115 units |
| UPC / GTIN / UDI-DI | 00811099011439 |
| Lot numbers | 807118, 807119, 807120, 811076 |
| Model numbers | 132-131D |
Product
TLS2 Thermal Ligating Shears, Catalog Number 132-131D
Reason for recall
The shears exhibited a high rate of complete or intermittent failure to actuate. As a result, they do not perform their intended function in surgical procedures.
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-1698-2019. 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.