Company
Aesculap AG
1 recall(s) on record — most severe on record: Class II.
| Owner-operator number | 8010193 |
|---|---|
| Registered facilities | 3 |
| Recalls on record | 1 |
Registered facilities (3)
- AESCULAP AG FEI 3002806315 · DE
- AESCULAP SAS FEI 3001354499 · FR
- B.Braun Medical (Suzhou) Co,.Ltd FEI 3008711893 · CN
Recalls & enforcement
- Class IIOngoing2025-08-18Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled as "Long" and the ELAN 4 FIXED DURAGUARD LONG was labeled as "Standard."
Watch this supplier
We'll email you when a new FDA recall or enforcement record is published for a facility you follow. (Inspection & warning-letter coverage is being added.)
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.