Home › The Alger Co Inc › ALGERBRUSH II
ALGERBRUSH II
The Alger Co Inc · Model BR2-1 · UDI-DI 00860005369201
0
510(k) clearances
0
Adverse events
1
Recalls
23
Facilities
Description
ALGERBRUSH II 1mm Complete Instrument, Carbide Burr
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-10-12 | Bausch & Lomb, Inc. | According to firm ( Bausch & Lomb, Inc. ) on June 17, 2016 a packaging operator notified his supervisor he had not placed the operating instruction into the last repackaging of SK |
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.