PlainRecalls
FDA Devices Moderate Class II Ongoing

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.

Reported: February 24, 2021 Initiated: December 30, 2020 #Z-1118-2021

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.

Details

Units Affected
7437480 units
Distribution
Worldwide distribution.
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
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.. Recalled by Baxter Healthcare Corporation. Units affected: 7437480 units.
Why was this product recalled?
complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 24, 2021. Severity: Moderate. Recall number: Z-1118-2021.