Drug recall
Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Access Tray with 0.025" Spring-Wire Guide…
FDA recall event 95228 · Class II · ARROW INTERNATIONAL Inc.
Key facts
| Event ID | 95228 |
|---|---|
| Recall numbers | Z-3299-2024 |
| Recalling firm | ARROW INTERNATIONAL Inc. |
| Product type | Devices |
| Products | Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Access Tray with 0.025" Spring-Wire Guide (Catheter Not Included), REF ASK-04001-BW1; (2) Arrow Arterial Access Tray with 0.021"… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Reports have been received regarding open seals on the packaging. |
| Initiation date | Jul 26, 2024 |
| Report date | Oct 2, 2024 |
| City | Morrisville |
| State | NC |
| Country | United States |
| FEI number | 3013162291 |
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: