PKG, 5MM INSERT, ENDO METZENBAUM SCISSORS, CURVED 45CM recall
PKG, 5MM INSERT, ENDO METZENBAUM SCISSORS, CURVED 45CM, P/N 0250080575 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and…
Why was PKG, 5MM INSERT, ENDO METZENBAUM SCISSORS, CURVED 45CM 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?
247425 345126 443972 542154 643084 744694 745080 745631 746499 747596 845622 940158 941057 942853 0943888E 0943889E 0945145E 0945724E 1040112E 1040803E 1041624E 1042486E 1042718E 1042721E 1043803E 1046698E 1142619E 1143800E 1145679E 1146359E 114635E 1146663E 1242122E 1242714E 1242919E 1243536E 1243952E 1244528E 1244582E 1244993E 1245516E 1246169E 1246647E 1340192 1340541 1343411 1343710 1344029 1344298 1345423 1345645 1346655 1440435 1440679 1441180 1441180E 1441815 1442256 1442808 1443226 1443650
- Product
- PKG, 5MM INSERT, ENDO METZENBAUM SCISSORS, CURVED 45CM, P/N 0250080575 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and…
- 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)