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Aesculap AG FDA Recalls
2 recalls on file across devices, 0 of them Class I and 2 still open. This firm is not matched to a listed company.
Newest first
Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.
| Product |
|---|
| AESCULAP ELAN 4 FIXED DURAGUARD STANDARD. Model Number: GB942R.Class IIAug 18, 2025Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled |
| AESCULAP ELAN 4 FIXED DURAGUARD LONG. Model Number: GB943R.Class IIAug 18, 2025Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled |