33cm Dorsey Grasper Forceps recall
33CM DORSEY GRASPER FORCEPS, P/N 0250080319. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue…
Why was 33cm Dorsey Grasper Forceps 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?
23600 247034 444470 542723 543906 641202 744068 747134 844302 940160 940347 943637 943669 944095 944199 944200 944217 945746 1040595 1040649 1040983 1042091 1042930 1042931 1042932 1042933 1045029 1045896 1045897 1140649 1141565 1141566 1142269 1143078 1143340 1144348 1144501 1144933 1144934 1145345 1145346 1145680 1145681 1146468 1146469 1146846 1146847 1240114 1240115 1241424 1241425 1241426 1242123 1242124 1242125 1242933 1242934 1245715 1245716 1245717 124597 1245974 1245975 1246057 1340291 1340715 1340716 1341252 1341834 1343135 1343534 1344250 1344498 1346554 1441858 250080319 383699 646009
- Product
- 33CM DORSEY GRASPER FORCEPS, P/N 0250080319. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue…
- 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)