PlainRecalls
FDA Devices Moderate Class II Ongoing

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis

Reported: December 4, 2024 Initiated: October 23, 2024 #Z-0560-2025

Product Description

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis

Reason for Recall

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

Details

Units Affected
22392 units
Distribution
Worldwide distribution.
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis. Recalled by Baxter Healthcare Corporation. Units affected: 22392 units.
Why was this product recalled?
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 4, 2024. Severity: Moderate. Recall number: Z-0560-2025.