FDA Device Intelligence
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Bausch + Lomb

Bausch & Lomb Incorporated · Model N2085 · UDI-DI 00757770417773

KAK Prescription
1
510(k) clearances
7
Adverse events
1
Recalls
93
Facilities

Description

PROBE SINUS SKILLERN GRADUATED

Recalls

DateFirmReason
2012-08-17Vital Signs Colorado Inc.There is a potential for epistaxis during use of the Disposable General Purpose 9 French Temperature Probe.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.