PKG, BABCOCK FORCEPS, P/N 0250080321. Laparoscopic recall
PKG, BABCOCK FORCEPS, P/N 0250080321. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs…
Why was PKG, BABCOCK FORCEPS, P/N 0250080321. Laparoscopic 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?
140571 140572 140590 442506 542896 643523 646838 741305 741307 744923 842628 842632 842638 842640 847869 847870 847872 847873 847877 847878 847880 847881 847885 847886 1041276 1042935 1042951 1045190 1046166 1046900 1046901 1140664 1140821 1142174 1142665 1143446 1143728 1144692 1145109 1146164 1146165 1146388 1146900 1146901 1147163 1240407 1240955 1241953 1241954 1242409 1243807 1244132 1244241 1244441 1245480 1246060 1246405 1340290 1341254 1341835 1341836 1343535 1343993 1346493 1440592 1440788 1440789
- Product
- PKG, BABCOCK FORCEPS, P/N 0250080321. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs…
- 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)