Arrow
7 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Arrow and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-05-20FDA-DeviceClass IArrow NextStep hemodialysis catheters recalled for sheath introducer failure
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.
- 2026-05-20FDA-DeviceClass IArrow International Cannon II Plus catheter recalled for sheath malfunction
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.
- 2026-05-20FDA-DeviceClass IArrow-Clark VectorFlow catheters recalled for introducer malfunction
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.
- 2026-05-20FDA-DeviceClass IArrow Edge hemodialysis kit recalled for sheath introducer defect
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.
- 2023-10-11FDA-DeviceClass IArrow Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30 days
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
- 2023-10-11FDA-DeviceClass ICheck Arrow ErgoPack Complete catheter kit labels
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
- 2023-10-11FDA-DeviceClass ICheck Arrow ErgoPack PICC catheter kits for labeling errors
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
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