FDA Device recall Z-1986-2014
Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221
- FDA Device
- Class II
- terminated
- Published 2014-07-09
On 2014-07-09 the FDA classified a Class II recall of Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221 by Microline Surgical, citing potential for the Fenestrated Grasper Tip jaw to break when force is applied to the jaw.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1986-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-05-12 |
| Published | 2014-07-09 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Microline Surgical |
| Distribution | CA, HI, ID, MA, MI, MS, PA, TN, TX, UT |
Product
Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221
Reason
Potential for the Fenestrated Grasper Tip jaw to break when force is applied to the jaw
Identifiers
| code_info | Lot Numbers: 00115342 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1986-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.