Class II
Medical Device Recall: EchoTip¿ Ultra Endoscopic Ultrasound Access Needle, ECHO-19, G31520
Cook Medical Incorporated · April 1, 2024
Reason for Recall
Devices may contain elevated levels of bacterial endotoxin.
Distribution
International distribution in the countries of Germany, Netherlands, Switzerland, United Kingdom.
States Affected
IN
Quantity Affected
8 units OUS
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1833-2024
Status: ongoing
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