Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips — Class II medical device recall Z-1987-2014
Terminated recall by Microline Surgical, Inc., reported 2014-07-09, distributed in CA, HI, ID, MA, MI, MS, PA, TN…. Potential for the Fenestrated Grasper Tip jaw to break when force is applied to the jaw
| Recall number | Z-1987-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microline Surgical, Inc., Beverly, MA, United States |
| Recall initiated | 2014-05-12 |
| Classified | 2014-07-02 |
| Reported by FDA | 2014-07-09 |
| Terminated | 2015-08-13 |
| Distributed | CA, HI, ID, MA, MI, MS, PA, TN, TX, UT |
| Countries outside the US | BE, CH, DE, FR, GB, ID, IE, KR, NO, SA, TR |
| Quantity | 6,290 units |
| Reason classes | device malfunction |
| Lot numbers | 00115282, 00115283, 00115284, 00115340, 00115341, 00115501, 00115502, 00115865, 00116277, 00116278 |
| Model numbers | 3222 |
Product
Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips (Reusable) Ref 3222
Reason for recall
Potential for the Fenestrated Grasper Tip jaw to break when force is applied to the jaw
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-1987-2014. 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.