Arrow recalls hemodialysis catheter kits with potential for improper splitting, causing pain, bleeding, or vessel injury. Affected kits include specific model numbers and lot codes.
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.
Arrow is recalling hemodialysis catheter kits that may not split correctly, leading to pain, bleeding, or vessel injury during procedures. This affects patients receiving dialysis treatments with the specified model numbers.
The 16F dual-valved splittable sheath introducer may not split as intended, causing withdrawal resistance, prolonged procedures, pain, bleeding, hematoma, tissue injury, or vessel wall injury. This can happen during dialysis treatments when the catheter is inserted.
Patients using hemodialysis treatments with the recalled catheter kits are most at risk. Healthcare providers who use these kits for dialysis procedures may also be affected.
Check the product reference numbers on the kit: CS-15242-I, CS-15282-I, or CS-15322-I. Look for specific lot codes like 30801902195280, 30801902195532, or 30801902197451.
Review the reference numbers and lot codes on the kit to confirm if it is affected.
The recalled kits have reference numbers CS-15242-I, CS-15282-I, and CS-15322-I with specific lot codes.
The 16F dual-valved splittable sheath introducer may not split as intended, causing withdrawal resistance, prolonged procedures, pain, bleeding, hematoma, tissue injury, or vessel wall injury.
The recall does not require immediate stop use; however, affected kits should be checked and replaced if they match the reference numbers and lot codes.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2156-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2156-2026 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.
