Class II — Microline Surgical, Inc.
| Recalling firm | MICROLINE SURGICAL, INC. |
|---|---|
| Registered facility | Microline Surgical, Inc (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | 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. |
| Product | TLS2 Thermal Ligating Shears, Catalog Number 132-131D |
| Quantity | 115 units |
| Distribution | The products were distributed to the following US states: ND and NY. The products were distributed to the following foreign countries: Germany, Netherlands. |
| Initiated | 2019-03-22 |
| Classified | 2019-05-31 |
| Terminated | 2020-07-30 |
| Recall number | Z-1698-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Microline Surgical, Inc. (Z-1698-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/82708/
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