FDA Device Intelligence
Home › BR Surgical, LLC › BR Surgical, LLC

BR Surgical, LLC

BR Surgical, LLC · Model BR42-61278 · UDI-DI 00840183515089

HNL
10
510(k) clearances
40
Adverse events
1
Recalls
155
Facilities

Description

BOWMAN Lacrimal Probe, cylindrical, stainless steel, size 7/8

Recalls

DateFirmReason
2015-02-26Quest Medical, Inc.Expiration date incorrectly printed in Manufacturing Date field on both pouch and carton labels

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 docs
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.