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 | Potential for the Fenestrated Grasper Tip jaw to break when force is applied to the jaw |
| Product | Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips (Reusable) Ref 3222 |
| Quantity | 6290 units |
| Distribution | Worldwide Distribution-USA including the states of CA, HI, ID, MA, MI, MS, PA, TN, UT, and TX. and the countries of Belgium, France, Ireland, Germany, Indonesia, Korea, Norway, Saudi Arabia, Switzerland, Turkey, and UK. |
| Initiated | 2014-05-12 |
| Classified | 2014-07-02 |
| Terminated | 2015-08-13 |
| Recall number | Z-1987-2014 |
| 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-1987-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/68495/
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