ARROW Endurance Extended Dwell Peripheral Catheter System — Class I medical device recall Z-1826-2023
Ongoing recall by ARROW INTERNATIONAL Inc., reported 2023-06-28, distributed nationwide. Potential for catheter separation or leakage
| Recall number | Z-1826-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | ARROW INTERNATIONAL Inc., Morrisville, NC, United States |
| Recall initiated | 2023-05-19 |
| Classified | 2023-06-21 |
| Reported by FDA | 2023-06-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 262,016 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 10801902132908, 10801902132922, 10801902132946, 10801902132960, 10801902132984, 10801902133004, 10801902133028, 10801902133042, 10801902133066, 10801902133080, 10801902144499, 10801902146318, 10801902192988, 10801902193022, 10801902196368, 10801902196375, 10801902196382, 10801902196399, 10801902196405, 10801902212105, 10801902212112 |
Product
ARROW Endurance Extended Dwell Peripheral Catheter System
Reason for recall
Potential for catheter separation or leakage
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1826-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.