Arrow Three-Lumen CVC — Class II medical device recall Z-1290-2022
Terminated recall by ARROW INTERNATIONAL Inc., reported 2022-07-06, distributed nationwide. Gravity flow rates on the affected product lidstock are incorrect.
| Recall number | Z-1290-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ARROW INTERNATIONAL Inc., Morrisville, NC, United States |
| Recall initiated | 2022-05-05 |
| Classified | 2022-06-27 |
| Reported by FDA | 2022-07-06 |
| Terminated | 2024-09-04 |
| Distributed | Nationwide (US) |
| Quantity | 10,301 units |
| UPC / GTIN / UDI-DI | 10801902136944, 10801902170856, 10801902179514, 20801902122838 |
| Lot numbers | 71F20A0430 |
| Model numbers | CV-12123-F |
Product
Arrow Three-Lumen CVC
Reason for recall
Gravity flow rates on the affected product lidstock are incorrect.
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-1290-2022. 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.