Drug recall
DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
FDA recall event 89117 · Class II · Medshape, INC.
Key facts
| Event ID | 89117 |
|---|---|
| Recall numbers | Z-0453-2022 |
| Recalling firm | Medshape, INC. |
| Product type | Devices |
| Products | DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The firm identified a nonconformance in Lot 04882 involving the endcap being manufactured to a longer length than indicated in product specifications, introducing the risk of the +6 mm endcap not… |
| Initiation date | Nov 17, 2021 |
| Report date | Jan 12, 2022 |
| City | Atlanta |
| State | GA |
| Country | United States |
| FEI number | 3007593722 |
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: