Home › Bausch & Lomb Incorporated › Bausch + Lomb
Bausch + Lomb
Bausch & Lomb Incorporated · Model SP7-05990B · UDI-DI 00757770407972
KAK
Prescription
1
510(k) clearances
7
Adverse events
1
Recalls
92
Facilities
Description
DILATOR 1.5MM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-08-17 | Vital Signs Colorado Inc. | There is a potential for epistaxis during use of the Disposable General Purpose 9 French Temperature Probe. |
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.