Data Foundry

Medical device recalls 2018

AGB+ Multi Lumen CVC Kit — Class II medical device recall Z-1335-2018

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 numberZ-1335-2018
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmArrow International Inc, Reading, PA, United States
Recall initiated2017-12-22
Classified2018-04-10
Reported by FDA2018-04-18
Terminated2020-05-27
DistributedDC
Countries outside the USBS, CA, MX, PA, SG
Reason classessterility
Lot numbers13F16L0220, 13F16M0173, 13F17B0031, 13F17B0035, 13F17B0135, 13F17B0224, 13F17C0414, 13F17C0470, 13F17D0191, 13F17D0243, 13F17D0275, 13F17D0325, 13F17E0142, 13F17E0358, 13F17E0463, 13F17E0626, 13F17E0627, 13F17E0685, 13F17E0830, 13F17F0049, 13F17F0169
Model numbersCDC-42703-B1A, CDC-42802-1A, CDC-42854-1A, CDC-45703-1A, CDC-45703-A1A, CDC-45703-B1A, CDC-45802-1A, CDC-45802-B1A, CDC-45854-1A, CDC-46702-1A, CDC-47702-1A

Product

AGB+ Multi Lumen CVC Kit (1) Part Number (PN): CDC-42703-B1A, (2) PN: CDC-42802-1A, (3) CDC-45703-1A, (4) CDC-45703-A1A, (5) PN: CDC-45703-B1A; AGB+ Quad-Lumen CVC Kit (6) PN: CDC-42854-1A, (7) PN: CDC-45854-1A; AGB+ Two-Lumen CVC Kit (8) PN: CDC-45802-1A, (9) PN: CDC-45802-B1A, (10) PN: CDC-46702-1A, (11) CDC-47702-1A; (12) Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features, PN: ASK-45703-AH

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-1335-2018. 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.