ARROWg+ard Blue¿ CVC Kit — Class II medical device recall Z-1333-2018

Terminated recall by Arrow International Inc, reported 2018-04-18, distributed in DC. Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot b

Recall number	`Z-1333-2018`
Product type	Medical device
Classification	Class II
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	Arrow International Inc, Reading, PA, United States
Recall initiated	2017-12-22
Classified	2018-04-10
Reported by FDA	2018-04-18
Terminated	2020-05-27
Distributed	DC
Countries outside the US	BS, CA, MX, PA, SG
Reason classes	sterility
Lot numbers	`13F16M0266`, `13F17A0017`, `13F17A0314`, `13F17B0037`, `13F17B0124`, `13F17B0345`, `13F17B0355`, `13F17C0484`, `13F17D0060`, `13F17E0451`, `13F17E0644`, `13F17E0727`, `13F17E0798`, `13F17E0799`, `13F17E0871`, `13F17F0291`, `13F17F0489`
Model numbers	`CDC-22123-1A`, `CDC-24301-1A`, `CDC-24306-1A`

Product

ARROWg+ard Blue¿ CVC Kit (1) Part Number (PN): CDC-24301-1A, (2) PN: CDC-24306-1A; (3) ARROWg+ard Blue¿ Large-Bore Multi-Lumen CVC Kit, PN: CDC-22123-1A; (4) Central Venous Catheterization Kit with Blue FlexTip(R) ARROWg+ard Blue(R) Catheter, Sharps Safety Features, and Maximal Barrier Precautions, PN: ASK-24301-GM; (5) Hemodialysis Catheterization Kit for High Volume Infusions, PN: CDC-25123-1A

Reason for recall

Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.

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-1333-2018. 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.