RecallRadar

FDA Device recall Z-0645-2015

PKG, MINI METZENBAUM SCISSORS, CURVED LONG, P/N 0250080266

On 2014-12-24 the FDA classified a Class II recall of PKG, MINI METZENBAUM SCISSORS, CURVED LONG, P/N 0250080266 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

AgencyFDA Device
Recall numberZ-0645-2015
ClassificationClass II
Statusterminated
Initiated2014-11-17
Published2014-12-24
Last updated2026-09-13 11:53 UTC
CompanyStryker Endoscopy
DistributionUS

Product

PKG, MINI METZENBAUM SCISSORS, CURVED LONG, P/N 0250080266. 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
644425 647618 740284 740286 740636 747707 846469 847448 847698 941706 942884 944092 945218 945721 945978…644425 647618 740284 740286 740636 747707 846469 847448 847698 941706 942884 944092 945218 945721 945978 1040106 1040384 1040591 1040980 1042651 1042652 1046111 1140150 1141221 1142911 1143081 1143802 1144941 1146981 1240108 1240979 1241812 1242922 1243456 1243541 1244535 12446651 1244709 1245454 1246133 1246651 1340100 1342147 1342763 1343294 1343295 1344295 1344525 1345290 1345421 1345528 1440445 1441381 1442043

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-0645-2015%22

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