Drug recall
Beaver EdgeAhead Stiletto/MVR Knife.90mm Straight (20G)-for ocular paracentesis incisions in cataract…
FDA recall event 91235 · Class II · Beaver Visitec International, Inc.
Key facts
| Event ID | 91235 |
|---|---|
| Recall numbers | Z-0782-2023 |
| Recalling firm | Beaver Visitec International, Inc. |
| Product type | Devices |
| Products | Beaver EdgeAhead Stiletto/MVR Knife .90mm Straight (20G)-for ocular paracentesis incisions in cataract procedures. Part Number: 376630 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Packaging sterile barrier has been compromised. Open seals can lead to a loss of device sterility and may lead to infection |
| Initiation date | Nov 30, 2022 |
| Report date | Jan 11, 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: