Gambro Cartridge Blood Set Prime Line, product code 101025 - Product Usage: intended for single u...

FDA Recall #Z-1118-2021 — Class II — December 30, 2020

Recall #Z-1118-2021 Date: December 30, 2020 Classification: Class II Status: Ongoing

Product Description

Gambro Cartridge Blood Set Prime Line, product code 101025 - Product Usage: intended for single use in a hemodialysis treatment using the Phoenix Dialysis Delivery Systems.

Reason for Recall

complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received.

Recalling Firm

Baxter Healthcare Corporation — Deerfield, IL

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

7437480 units

Distribution

Worldwide distribution.

Code Information

UDI 07332414007836, All lots within expiry

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated