Drug recall
RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Usage: The single use injectors (Model STWOl and…
FDA recall event 85270 · Class II · Rayner Intraocular Lenses Limited
Key facts
| Event ID | 85270 |
|---|---|
| Recall numbers | Z-1753-2020 |
| Recalling firm | Rayner Intraocular Lenses Limited |
| Product type | Devices |
| Products | RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Usage: The single use injectors (Model STWOl and Model RSPOl) are intended to be used to compress and insert into the capsular bag only those… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | RaySert PLUS RSP01 LOT K030 labeled with an expiry of 2024-01 contained an inner tray that was labeled with an expiry of 2015. In addition to having an expiry of 2015 the LOT number on the inner tray… |
| Initiation date | Mar 17, 2020 |
| Report date | Apr 29, 2020 |
| City | Worthing |
| Country | United Kingdom |
| FEI number | 3002809583 |
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: