fda_recall · device_recall · critical
ARROW INTERNATIONAL, LLC — Class I recall: Arrow Edge Hemodialysis Catheterization Product, REF: CS-15242-I, CS-15282-I, CS…
- Event date
- 2026-05-20 00:00:00Z
- Observed
- 2026-07-09 22:52:29Z
- Source ID
- Z-2156-2026
- Payload hash
- e8588309f3e6b4793a5c2cd9…
Summary
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 inju… Status: Ongoing.
Entities
Informational only. Not legal, financial, or medical advice.