Arrow recalls specific Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kits due to potential inadequate connection between Micro Clave Clear Connectors and the kit, which could lead to improper use.
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.
Arrow is recalling certain Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kits because the Micro Clave Clear Connectors might not connect properly with the kit. This could lead to improper use during medical procedures.
The Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit may not connect adequately with the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit. This could lead to improper use during medical procedures, potentially causing complications.
Healthcare professionals using the recalled CVC kits are most at risk. Patients receiving these kits may also be affected if the connectors fail to connect properly.
Check for the product's REF numbers: ASK-42703-NS, ASK-42703-PCCH2, ASK-42703-PUPM1, ASK-45703-NS, ASK-45703-PAU, ASK-45703-PCAM1, ASK-45703-PCCH2, or ASK-45703-PN. The kits also have specific lot numbers and UDI/DI codes listed in the recall notice.
Review the product's REF numbers and lot numbers to confirm if it is recalled.
The recalled kits have REF numbers: ASK-42703-NS, ASK-42703-PCCH2, ASK-42703-PUPM1, ASK-45703-NS, ASK-45703-PAU, ASK-45703-PCAM1, ASK-45703-PCCH2, or ASK-45703-PN.
Check for the specific REF numbers and lot numbers listed in the recall notice.
The recall notice does not specify a remedy, so contact Arrow International for further instructions.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0352-2023 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0352-2023 from Arrow. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
