Access Vascular, Inc Recall: HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for
Access Vascular, Inc Recall: HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Access Vascular, Inc; Product: HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (<30days) to the peripheral venous acc
| Recalling firm | Access Vascular, Inc |
|---|---|
| Product | HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (<30days) to the peripheral venous access system for intravenous therapy Product Model Number: 80004004 |
| Reason for recall | Product Mislabeled on the outer bag and inner kit Tyvek header bag |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | US Nationwide distribution in the states of FL, TX, WA. |
| Recall initiated | 20221222 |
| Recall number | Z-1155-2023 |
| Category | device |
| State | MA |
| Country | United States |
$29/mo
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