Drug recall
1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses
FDA recall event 79152 · Class II · Johnson & Johnson Vision Care, Inc.
Key facts
| Event ID | 79152 |
|---|---|
| Recall numbers | Z-1209-2018, Z-1210-2018, Z-1211-2018 |
| Recalling firm | Johnson & Johnson Vision Care, Inc. |
| Product type | Devices |
| Products | 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses, ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR, ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil. |
| Initiation date | Oct 19, 2017 |
| Report date | Apr 4, 2018 |
| Termination date | Jun 12, 2020 |
| City | Jacksonville |
| State | FL |
| Country | United States |
| FEI number | 1000222023 |
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: