Drug recall
Sure T, contact, contact detach, neria, neria detach, neria multi and thalaset Used in combination with…
FDA recall event 71332 · Class II · Unomedical As
Key facts
| Event ID | 71332 |
|---|---|
| Recall numbers | Z-1821-2015 |
| Recalling firm | Unomedical As |
| Product type | Devices |
| Products | Sure T, contact, contact detach, neria, neria detach, neria multi and thalaset Used in combination with infusion pumps for continuous subcutaneous infusion of medication. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Unomedical has found that in rare cases the steel needle can break during use, interrupting the delivery of medication including insulin. |
| Initiation date | May 21, 2015 |
| Report date | Jul 1, 2015 |
| Termination date | Jan 23, 2017 |
| City | Roskilde |
| Country | Denmark |
| FEI number | 3004036962 |
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: