PKG, 5MM INSERT, RIGHT ANGLE FORCEP, 33CM, P/N recall
PKG, 5MM INSERT, RIGHT ANGLE FORCEP, 33CM, P/N 0250080694 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating…
Why was PKG, 5MM INSERT, RIGHT ANGLE FORCEP, 33CM, P/N recalled?
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 should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
44493 647221 647992 745498 842129 845882 846787 847844 940092 940153 941265 941741 944824 1040124 1040628 1041467 1042526 1042527 1043031 1043779 10441058 1044108 1045039 1045371 1046186 1046395 1046955 1047068 1140260 1141156 1141790 1142614 1144485 1145002 1145148 1145969 1146672 1240949 1241420 1241798 1242459 1243202 1244181 1244438 1244527 1244594 1245525 1245545 1246645 1340475 1341523 1342388 1343130 1343554 1344027 1344278 1344686 1346102 1440693 1441635 1443223
- Product
- PKG, 5MM INSERT, RIGHT ANGLE FORCEP, 33CM, P/N 0250080694 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating…
- Recalling firm
- Stryker Endoscopy
- Quantity
- 180,573 units total
- 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.
- Recall date
- December 24, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)