Home › Aesculap AG › AESCULAP
AESCULAP
Aesculap AG · Model BB063R · UDI-DI 04038653137459
EMO
Prescription
0
510(k) clearances
0
Adverse events
1
Recalls
62
Facilities
Description
Scalpel Handle, 5 3/4", (145 mm), round handle, non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-03-28 | Ace Surgical Supply Co., Inc. | The product inside the package is incorrect. A single blade shoe was mistakenly packaged instead of a double blade. |
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.