Home › Aesculap AG › AESCULAP
AESCULAP
Aesculap AG · Model MB285R · UDI-DI 04046963365448
HXD
Prescription
10
510(k) clearances
1,235
Adverse events
4
Recalls
336
Facilities
Description
DIETHRICH Bulldog Clamp, straight, 2 1/4", (55 mm), serrated, (13 mm), micro, non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | Aesculap Inc | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. |
| 2024-02-23 | MEDLINE INDUSTRIES, LP - Northfield | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. |
| 2018-05-04 | Stryker GmbH | Laser etching which indicates whether the device is in compression or distraction mode appears to be on the wrong side of the lever arm |
| 2015-06-16 | Symmetry Surgical, Inc. | Lack of sterility assurance. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.