Drug recall
Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA05100 Product Usage: Recommended for use in…
FDA recall event 81460 · Class II · Numed Inc
Key facts
| Event ID | 81460 |
|---|---|
| Recall numbers | Z-0510-2019, Z-0511-2019 |
| Recalling firm | Numed Inc |
| Product type | Devices |
| Products | Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA05100 Product Usage: Recommended for use in catheterization for angiography of cardiovascular vessels and I or chambers. It can be used for…, Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA06100 Product Usage: Recommended for use in catheterization for angiography of cardiovascular vessels and I or chambers. It can be used for… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Instructions for Use booklets were not included on the outer pouch |
| Initiation date | Oct 17, 2018 |
| Report date | Dec 5, 2018 |
| Termination date | Jan 28, 2019 |
| City | Hopkinton |
| State | NY |
| Country | United States |
| FEI number | 1318694 |
At a glance
- 1–9 Products in this recall
- 10–99 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: