Arrow 8 — Class II medical device recall Z-2556-2019
Terminated recall by Arrow International Inc, reported 2019-10-02, distributed nationwide. Products may contain the incorrect banner card within the kit
| Recall number | Z-2556-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2019-08-06 |
| Classified | 2019-09-23 |
| Reported by FDA | 2019-10-02 |
| Terminated | 2020-09-29 |
| Distributed | Nationwide (US) |
| Quantity | 231 units |
| Lot numbers | 13F18H0499 |
Product
Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.
Reason for recall
Products may contain the incorrect banner card within the kit
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-2556-2019. 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.