Inability to advance the guidewire through the feeding tube during placement due to blocked lumen of the barb connector. May lead prolongation in the procedure to exchange the device for another leading to leading to a cascade of events which may include additional intervention to close the puncture site, bleeding, leakage of gastric contents, and aspiration
Reason for recall: Inability to advance the guidewire through the feeding tube during placement due to blocked lumen of the barb connector. May lead prolongation in the procedure to exchange the device for another leading to leading to a cascade of events which may include additional intervention to close the puncture site, bleeding, leakage of gastric contents, and aspiration Distribution: Worldwide distribution - US Nationwide and the country of Japan. Quantity: 2501 units Lot/code info: GTIN: 08714729802631 Lot Numbers: 32295181 , 32295182 , 32306054 , 32306055 , 32316800 , 32323673 , 32342013 ,32367049 , 32367050 , 32374782 , 32472868 , 32486230 , 32486231 , 32486232 , 32486233 , 32506056 , 32515039 , 32523243 , 32523244 , 32531793 , 32531794 , 32531795 , 33113026 , 33113027 , 33113028 , 33113029 , 33170338
08714729802631
Official record: FDA (Device enforcement) ↗
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