Arrow recalls pressure injectable central venous catheters with incorrect adhesive manufacturing. Affected models include ArrowG+ard and ArrowG+ard Blue Plus with specific UDI codes. No immediate action needed but check for the listed batch numbers.
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Arrow is recalling certain pressure injectable central venous catheters due to a supplier issue with the liquid adhesive. This could lead to improper catheter function or infection risks if used incorrectly. Patients should check their catheter's UDI code and batch number to see if it's affected.
The liquid adhesive was incorrectly manufactured by a supplier, which may cause the catheter to malfunction or increase infection risk. The catheter is designed for short-term use to prevent bloodstream infections but not for treating existing infections.
Healthcare providers and patients using ArrowG+ard or ArrowG+ard Blue Plus pressure injectable catheters with specific UDI codes and batch numbers are affected. Those with catheters from the listed batches are at the highest risk.
Check the UDI code on the catheter label for the specific batch numbers listed: 33F25L0140, 33F25L0143, 33F25L0144, or 33F25L0145. The product codes are ASK-42802-PLH, ASK-45703-MGH, ASK-42854-MGH, or ASK-45854-MGH.
Look for the UDI code on the catheter label to determine if it matches the listed batch numbers: 33F25L0140, 33F25L0143, 33F25L0144, or 33F25L0145.
The liquid adhesive was incorrectly manufactured by a supplier, which may cause the catheter to malfunction or increase infection risk.
Check the UDI code on the catheter label for the specific batch numbers listed: 33F25L0140, 33F25L0143, 33F25L0144, or 33F25L0145.
The catheter is designed for short-term use to prevent bloodstream infections but not for treating existing infections. If it's not affected by the recall, it should be safe to use as intended.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1914-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1914-2026 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.
