Aesculap AG Recalls

2 recalls found for Aesculap AG. Check if any of your products are affected.

HIGHFDA DEVICE

Aesculap AG Recalls Surgical Instrument Due to Mislabeling

Aesculap AG recalled three surgical instruments on August 18, 2025, due to mislabeling issues. The ELAN 4 FIXED DURAGUARD LONG was incorrectly labeled as "Standard" and vice versa. The recall affects devices distributed in the U.S. and several international markets.

Aesculap AG
Mislabeling. The
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Brand Statistics

Total Recalls
2
Pages
1