EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR: recall status
⚠ Recalls found. EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR is named in 2 official recalls in our current data:
FDA Class II recall Z-2806-2026 — Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dysfunction.
FDA Class II recall Z-2807-2026 — Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dysfunction.
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…