The FDA has posted 10 enforcement recalls from Aesculap Inc since 2025, none of them Class I (most serious). Most recent report: Mar 11, 2026.
There is the potential for the length of the trocar shaft to be too long.
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Firm name as filed with the FDA: “Aesculap Inc”. Related firm entities may file under separate names. Source: U.S. FDA openFDA device enforcement reports. Informational only — verify with the FDA before acting.