PKG, 10MM CLIP APPLYING FORCEPS, P/N 0250080558. recall
PKG, 10MM CLIP APPLYING FORCEPS, P/N 0250080558. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of…
Why was PKG, 10MM CLIP APPLYING FORCEPS, P/N 0250080558. 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?
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
- Product
- PKG, 10MM CLIP APPLYING FORCEPS, P/N 0250080558. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of…
- 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)