Health & Personal Care
HIGH
FDA DEVICE
Aesculap MINOP TROCAR 150MM Recall for 126 Units in 2026
Aesculap recalls 126 MINOP TROCAR 150MM devices distributed nationwide to U.S. hospitals and clinics after regulators flagged a shaft length issue. The shaft may be longer than specified, potentially harming tissue during procedures. Healthcare facilities should stop using the devices and follow manufacturer recall instructions immediately.
Aesculap
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