Drug recall
TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in…
FDA recall event 87320 · Class II · Johnson & Johnson Surgical Vision Inc
Key facts
| Event ID | 87320 |
|---|---|
| Recall numbers | Z-1163-2021 |
| Recalling firm | Johnson & Johnson Surgical Vision Inc |
| Product type | Devices |
| Products | TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in the capsular bag. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Due to the release of nonconforming Intraocular Lenses (IOLs). |
| Initiation date | Jan 27, 2021 |
| Report date | Mar 10, 2021 |
| Termination date | Nov 9, 2022 |
| City | Santa Ana |
| State | CA |
| Country | United States |
| FEI number | 3003843509 |
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: