PKG, ATRAUMATIC FORCEPS, DOUBLE ACTION, P/N 0250080311. recall
PKG, ATRAUMATIC FORCEPS, DOUBLE ACTION, P/N 0250080311. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating…
Why was PKG, ATRAUMATIC FORCEPS, DOUBLE ACTION, P/N 0250080311. 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?
44035 140782 244776 245545 343856 441524 442997 540455 544016 544024 646306 646310 646312 646314 646317 646318 747599 747602 747604 747605 747608 840082 8460129 846018 846019 846023 846024 846025 846029 846030 846031 846032 846034 846035 940559 940560 940561 940562 940563 940564 940565 940566 940567 940568 940570 940571 940572 940573 1042186 1042190 1042191 1042192 1042193 1042194 1042195 1042196 1042197 1042198 1042199 1042200 1042201 1043521 1043522 1043523 1046150 1142193 1142194 1144246 1144247 1144936 1144997 1145107 1145223 1146160 1146699 1146700 1146701 1146840 1241180 1241402 1241403 1242704 1242705 1242837 1243090 1243158 1243587 1244005 1244006 1245513 1246061 1246188 1246189 1246190 1340491 1340492 1340712 1340713 1341440 1341837 1341838 1341839 1342205 1342847 1343136 1344422 1345089 1346207 1440342 1440343 1440344 1441218 1441464 641979
- Product
- PKG, ATRAUMATIC FORCEPS, DOUBLE ACTION, P/N 0250080311. 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)