FDA Device recall Z-0652-2015
PKG, MARYLAND FORCEPS, CURVED LEFT, P/N 0250080282
- FDA Device
- Class II
- terminated
- Published 2014-12-24
On 2014-12-24 the FDA classified a Class II recall of PKG, MARYLAND FORCEPS, CURVED LEFT, P/N 0250080282 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-0652-2015 |
| 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, MARYLAND FORCEPS, CURVED LEFT, P/N 0250080282. 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 | 43967 140297 246217 340634 341506 341508 344540 344549 444519 05242012E 542134 641033 641039 646904 64692…43967 140297 246217 340634 341506 341508 344540 344549 444519 05242012E 542134 641033 641039 646904 646920 646927 646929 647553 741526 747007 747010 747012 747017 747023 747024 846041 846044 846048 846060 846061 846062 846080 941874 941876 941877 941878 941879 941880 941881 941885 941886 941887 941888 941889 941890 941894 941895 941897 941898 941899 941900 941904 941905 941906 942385 945570 945571 945572 945573 945574 945575 945576 945580 945581 945582 945585 945586 945587 945591 945592 945594 945595 945596 945597 945601 945602 945603 1045189 1045364 1045365 1045366 1045675 1045676 1045677 1045678 1045679 1046174 1046612 1046613 1140665 1140666 1140667 1140668 1140669 1141746 1141747 1142170 1142171 1142172 1142185 1142186 1142187 1142631 1142632 1143459 1143460 1143461 1143462 1143463 1143464 1143465 1144713 1144714 1144715 1144716 1144717 1144721 1145476 1145477 1146 |
|---|
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-0652-2015%22
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