Drug recall
STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses.
FDA recall event 74067 · Class II · Staar Surgical Co.
Key facts
| Event ID | 74067 |
|---|---|
| Recall numbers | Z-1964-2016 |
| Recalling firm | Staar Surgical Co. |
| Product type | Devices |
| Products | STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The STAAR AQ Cartridge-FP may malfunction and may crack during loading or delivery of the IOL (Intraocular Lenses). |
| Initiation date | May 2, 2016 |
| Report date | Jun 22, 2016 |
| Termination date | Nov 15, 2016 |
| City | Monrovia |
| State | CA |
| Country | United States |
| FEI number | 2023826 |
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 · Source date: