Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit — Class I medical device recall Z-0352-2023

Terminated recall by ARROW INTERNATIONAL Inc., reported 2022-12-21, distributed in FL, GA, KY, OH, PA, WV. There is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear

Recall number	`Z-0352-2023`
Product type	Medical device
Classification	Class I
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	ARROW INTERNATIONAL Inc., Morrisville, NC, United States
Recall initiated	2022-10-27
Classified	2022-12-09
Reported by FDA	2022-12-21
Terminated	2024-10-07
Distributed	FL, GA, KY, OH, PA, WV
Quantity	1,275 units
UPC / GTIN / UDI-DI	`10801902140675`, `10801902141030`, `10801902141047`, `10801902159110`, `10801902159592`, `10801902162905`, `10801902162912`, `10801902203158`
Lot numbers	`13F22B0021`, `13F22B0495`, `13F22B0641`, `13F22C0244`, `13F22C0350`, `13F22C0553`, `13F22C0862`, `13F22D0121`

Product

Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c) ASK-42703-PUPM1, d) ASK-45703-NS, e) ASK-45703-PAU, f) ASK-45703-PCAM1, g) ASK-45703-PCCH2, h) ASK-45703-PN; catheter introducer

Reason for recall

There is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit and the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC 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-0352-2023. 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.