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All product recalls associated with Ethicon Endo-Surgery Inc.
Total Recalls
1000
Past Year
421
Class I (Serious)
53
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The firm initiated this second subsequent recall because the affected devices can remain closed and clamped on tissue during surgical procedures due to the fact that the mechanism which connects the articulation joint to the device shaft is insufficient.
Software anomalies may allow the image orientation to be misinterpreted, posing a potential patient safety issue.
A defect in the AEC board in the system's control causes failure to terminate additional exposures at the exposure time selected for the initial exposure.