Drug recall
CustomEyes kits
FDA recall event 91488 · Class II · Beaver Visitec International, Inc.
Key facts
| Event ID | 91488 |
|---|---|
| Recall numbers | Z-1199-2023, Z-1200-2023 |
| Recalling firm | Beaver Visitec International, Inc. |
| Product type | Devices |
| Products | CustomEyes kits, Ultracell Wick with 80cc Collection Bag, 20/box |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Device packaging may contain open seals, compromising product sterility. |
| Initiation date | Dec 20, 2022 |
| Report date | Mar 8, 2023 |
| City | Waltham |
| State | MA |
| Country | United States |
| FEI number | 1211998 |
At a glance
- 1–9 Products in this recall
- 1–9 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: