FDA Device recall Z-0721-2015
PKG, 10MM PEEK MONOPOLAR HANDLE, P/N 0250080618 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulatin…
- FDA Device
- Class II
- terminated
- Published 2014-12-24
On 2014-12-24 the FDA classified a Class II recall of PKG, 10MM PEEK MONOPOLAR HANDLE, P/N 0250080618 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulatin… 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-0721-2015 |
| 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, 10MM PEEK MONOPOLAR HANDLE, P/N 0250080618 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 | 42167 42169 42172 43238 43239 81309 142647 143476 143477 245841 342652 344115 345130 0442468C 0445112D 0…42167 42169 42172 43238 43239 81309 142647 143476 143477 245841 342652 344115 345130 0442468C 0445112D 0541360D 0541361D 0641114D 0641115D 0644773D 0645377D 0647994D 06CON06071 06CON06126 07022013E 0740507D 0740834D 0741766D 0742442D 0742740D 0744063D 0744684D 0745499D 0746059D 0746497D 0747592D 0840357D 0840678D 0841358D 0842085D 0842130D 0845885D 0846565D 0847512D 9292011 0940124D 0940126D 0940127D 0941052D 0941067D 0942146D 0942277D 0942850D 0943496D 0944142D 0945209D 0945467D 0945715D 1040120D 1040385D 1040583D 1040805D 1041471D 1041627D 1041982D 1042493D 1043025D 1043102D 1043511D 1043778D 1044521D 1044523D 1046109D 1046189D 1046193D 1141605D 1141791D 1142149D 1142927D 1143476D 1143648D 1143972D 1144238D 1144345D 1144346D 1144395D 1144642D 1144656D 1144961D 1145073D 1145344D 1145810D 1145941D 1146537D 1146660D 1146661D 1240125D 1240950D 1241422D 1241512D 1242235D 1242642D 1242713D |
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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-0721-2015%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.