Drug recall
Brimonidine Tartrate Ophthalmic Solution 0.2% (Sterile), Each mL Contains Active: Brimonidine tartrate 0.2%…
FDA recall event 61261 · Class III · Bausch & Lomb, Inc.
Key facts
| Event ID | 61261 |
|---|---|
| Recall numbers | D-1263-2012 |
| Recalling firm | Bausch & Lomb, Inc. |
| Product type | Drugs |
| Products | Brimonidine Tartrate Ophthalmic Solution 0.2% (Sterile), Each mL Contains Active: Brimonidine tartrate 0.2% (Sterile), 15 mL bottles, Rx only, Bausch & Lomb Incorporated Tampa, FL 33637 ---- NDC… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Impurity/Degradation; 9 month stability |
| Initiation date | Feb 22, 2012 |
| Termination date | Jul 3, 2012 |
| City | Tampa |
| State | FL |
| Country | United States |
| FEI number | 1000113778 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports