Unomedical A/S Recall: Neria Soft Infusion Set, Product Code 507302, intravascular adminis
Unomedical A/S Recall: Neria Soft Infusion Set, Product Code 507302, intravascular adminis is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Unomedical A/S; Product: Neria Soft Infusion Set, Product Code 507302, intravascular administration set; Reason for recall: Specific lots of Neria
| Recalling firm | Unomedical A/S |
|---|---|
| Product | Neria Soft Infusion Set, Product Code 507302, intravascular administration set |
| Reason for recall | Specific lots of Neria Soft Infusion Sets, which have been shipped into the US Market, have been shipped with the incorrect Instruction for Use (IFU) within the final pack. The IFU included is the IFU registered for the Rest of World (ROW) countries. The difference between the US IFU and the ROW IFU is the addition of an intended use section in the ROW IFU. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | US Nationwide distribution in the state of Florida. |
| Recall initiated | 20240305 |
| Recall number | Z-1544-2024 |
| Category | device |
| Country | Denmark |
$29/mo
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