Home › Bausch & Lomb Incorporated › Bausch + Lomb
Bausch + Lomb
Bausch & Lomb Incorporated · Model E3096L 9.50 · UDI-DI 10757770055804
HRH
Prescription
10
510(k) clearances
23
Adverse events
1
Recalls
122
Facilities
Description
Trephine Blade
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-05-03 | Surgical Instrument Service And Savings, Inc. | The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch. |
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.