Devices

Device Recall PKG, 10MM CLIP APPLYING FORCEPS

Model / Serial
542717 843041 847479 847627 847629 848038 940795 941317 941318 941593 941795 943083 943448 945440 1042080 1042461 1043112 1043518 1043519 1043822 1044267 1044668 1045044 1045156 1045157 1045635 1046403 1047041 1140146 1141380 1141391 1142161 1142936 1144221 1144338 1144339 1144586 1145064 1145691 1146117 1147033 1147093 1240138 1240542 1240943 1240944 1241414 1242116 1242450 1242639 1246203 1340114 1341612 1342005 1342780 1344203 1345233 1345803 1346548 1346656 1440681
Device Class
2
Implanted device?
No
Distribution
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.
Product Description
PKG, 10MM CLIP APPLYING FORCEPS, P/N 0250080558. || 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.
Manufacturer
Stryker Endoscopy
1 Event
- Recall of Device Recall PKG, 10MM CLIP APPLYING FORCEPS

Manufacturer

Stryker Endoscopy

Manufacturer Address
Stryker Endoscopy, 5900 Optical Ct, San Jose CA 95138-1400
Manufacturer Parent Company (2017)
Stryker
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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