FDA Recall Open, Classified

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.

Recall: Z-1118-2021 · Initiated December 30, 2020

Recall

Recall Number
Z-1118-2021
Event Number
87150
Firm
Baxter Healthcare Corporation
FEI Number
1417572
Product Code
FJK
Status
Open, Classified
Root Cause
Under Investigation by firm
Initiated
December 30, 2020
Address
1 Baxter Pkwy, Deerfield, IL, 60015-4625

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

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

Action

The firm issued a Safety Alert on 12/30/2020 by mail. The letter explained the problem with photographs, and the hazard involved with using a device with a kinked line. Customers identifying set with kinked tubing may contact Baxter Healthcare Center for Service to arrange for return and credit. Baxter Healthcare Center for Service can be reached at 888-229-0001 between the hours of 7:00 am and 6:00 pm Central Time, Monday through Friday. Distributor were asked to notify their customers by distributing the letter.

Distribution

Worldwide distribution.

Quantity

7437480 units