Drug recall
ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
FDA recall event 89928 · Class II · Carl Zeiss Meditec AG
Key facts
| Event ID | 89928 |
|---|---|
| Recall numbers | Z-1007-2022 |
| Recalling firm | Carl Zeiss Meditec AG |
| Product type | Devices |
| Products | ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | High friction of the slider can cause the device to stick, or not move as intended. |
| Initiation date | Mar 16, 2022 |
| Report date | May 4, 2022 |
| City | Oberkochen |
| Country | Germany |
| FEI number | 3003481798 |
At a glance
- 1–9 Products in this recall
- None 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: