FDA Device recall Z-0689-2015
PKG, NEEDLE HOLDER, STRIAGHT, P/N 0250080340
- FDA Device
- Class II
- terminated
- Published 2014-12-24
On 2014-12-24 the FDA classified a Class II recall of PKG, NEEDLE HOLDER, STRIAGHT, P/N 0250080340 by Stryker Endoscopy, citing the parameters provided in the Laparoscopic Manual Instruments Instructions for Use (IFU 1000-401-070 Revision G or prior) do not support the unwrapped Gravity cycle and the Ethyl….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0689-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-11-17 |
| Published | 2014-12-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Stryker Endoscopy |
| Distribution | US |
Product
PKG, NEEDLE HOLDER, STRIAGHT, P/N 0250080340. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them to be used for electrosurgery. Laparoscopic surgical manual instruments are designed to be used endoscopically through cannulae to perform cutting, grasping, dissecting, retracting, and manipulating functions. This device does not sustain or support life.
Reason
The parameters provided in the Laparoscopic Manual Instruments Instructions for Use (IFU 1000-401-070 Revision G or prior) do not support the unwrapped Gravity cycle and the Ethylene Oxide cycle sterilization methods
Identifiers
| code_info | 247810 341537 440293 441251 441512 742141 744846 745483 840074 840509 846996 847695 847971 940051 940785…247810 341537 440293 441251 441512 742141 744846 745483 840074 840509 846996 847695 847971 940051 940785 941250 942774 943684 944126 945441 1040422 1042501 1042937 1043498 1045032 1045646 1046195 1140658 1141568 1141927 1142299 1144210 1144626 1145149 1145983 1146678 1240546 1242127 1242255 1242935 1243538 1243953 1245819 1246065 1246178 1341532 1341556 1342750 1343397 1344034 1344462 1345425 1346314 1440438 1440466 1443606 |
|---|
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-0689-2015%22
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