FDAFDA · Food and drugs·Recall number Z-0622-2015
PKG, ROTATING HANDLE, RATCHET, INSULATED SHAFT, P/N 0250080231. 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.
Published December 24, 2014 · Recall initiated: November 17, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Stryker Endoscopy
- Distributor
- Worldwide Distribution - USA (nationwide) and Internationally to Algeria, Argentina, Australia, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Ecuador, France, Germany, Greece, Guam, Guatemala, India, Italy, Japan, Jordan, Kuwait, Latin America, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Peru, Philippines, Poland, Portugal, Puerto Rico, Romania, Saudi Arabia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Turkey, United Arab Emirates, United Kingdom, and Venezuela.
- Lot
- 141317 142334 246391 341054 341055 04102012E 540683 540685 0541433D 0541434D 6172014 0640767D 0644142D 0647413D 0647616D 0742463D 0743206D 0744706D 0745084D 0746367D 0747892D 08152012E 08426254D 0845326D 0845889D 0846254D 0847431D 0940080D 0940786D 0942136D 0944434D 0944806D 0945985D 1040597D 1040799D 1041469D 1042944D 1043499D 1143128D 1145076D 1145982D 1147040D 1245448 1245519 1245737 1246194 1246197 1341543 1341543D 1341568 1341568D 1344132 1344132D 1344679 13446790 1344679D 1345511 1442519
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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