Arrow recalls Cannon II Plus hemodialysis catheters with specific model numbers due to potential sheath splitting issues causing pain, bleeding, and vessel injury during dialysis procedures.
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 certain Cannon II Plus hemodialysis catheters that may not split as intended. This can lead to prolonged procedure times, pain, bleeding, hematoma, or vessel injury during dialysis treatments.
The 16F dual-valved splittable sheath introducer in the catheter may not split properly during use. This can cause increased resistance when withdrawing the catheter, leading to longer procedures, pain, bleeding, hematoma formation, or damage to blood vessels.
Patients using hemodialysis treatments with the recalled catheters are most at risk. Healthcare providers who use these catheters for dialysis procedures may also be affected.
Check for model numbers CS-15242-VSP, CS-15282-VSP, CS-15322-VSP, CS-15362-VSP, or CS-15552-VSP on the catheter packaging or label. The catheter may also have a specific lot number or serial code listed in the product description.
Look for model numbers CS-15242-VSP, CS-15282-VSP, CS-15322-VSP, CS-15362-VSP, or CS-15552-VSP on the catheter packaging or label.
If you have the recalled catheter, contact your healthcare provider to discuss alternative options or potential risks.
The affected model numbers are CS-15242-VSP, CS-15282-VSP, CS-15322-VSP, CS-15362-VSP, CS-15552-VSP, CSD-15242-SP, CSD-15282-SP, CS-15242-SPM, CS-15282-SPM, CS-15322-SPM, and CS-15362-SPM.
The 16F dual-valved splittable sheath introducer may not split as intended, which can cause withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, or vessel injury during dialysis.
Contact your healthcare provider to discuss alternative options or potential risks. They will advise on the next steps based on your specific situation.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2158-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2158-2026 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.
