Arrow recalls specific Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC Kits due to incorrect adhesive manufacturing. This may affect catheter infection prevention safety.
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Arrow is recalling certain Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC Kits because the liquid adhesive was incorrectly manufactured. This could impact the catheter's ability to prevent bloodstream infections. Affected users should check their product codes and contact Arrow for details.
The recall is due to a supplier notice about incorrect adhesive manufacturing. This could compromise the catheter's effectiveness in preventing bloodstream infections. However, the specific risk to users is not clearly described in the recall notice.
Healthcare professionals using the Arrowg+ard Blue Plus catheters for central venous catheter (CVC) systems are most at risk. Patients receiving these catheters for short-term use may also be affected.
Check for the product code ASK-45854-PUPM1 with UDI code (01)10801902159578(17)270531(11)251205(10)33F25M0011 or batch number 33F25M0011. Also look for other product codes with matching UDI and batch numbers listed in the recall.
Identify your Arrowg+ard Blue Plus catheter's product code and UDI code to confirm if it is affected.
The recall is due to a supplier notice that the liquid adhesive was incorrectly manufactured.
The recall notice does not specify a remedy, so contact Arrow directly for instructions.
The recall notice does not provide details on the specific risk to users.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1915-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1915-2026 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.
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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.
