WhichRecall
Class IIReported 2026-03-04

Convenience kits containing Tego Connectors Medline DIALYSIS DRSNG CHNG SKU DYNDC3167

Recalled by Medline Industries, LP

Reason for Recall

Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits

Advertisement

Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.

Recall Number
Z-1468-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2026-01-08
Reported
2026-03-04
Distribution
US Nationwide distribution.
Code Info
UDI-DI (ea) 10195327015954 UDI-DI (case) 40195327015955 Kit lots 24IME953 25CMA708
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
Advertisement