Official recall notice

FDA DeviceClass INotable

FDA Recall: Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administratio

Recall date
2026-08-19
FDA class
Class I

Why it was recalled

Hazard

Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open position.

Recommended action

What to do

24528 units

Product description

Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open position.

Verify with the official notice →
Share:

Related Recalls

2026-07-08 · FDA_DEVICE
FDA Recall: Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Circuit), Model/Catalog Number REF M08270;
Baxter Healthcare Corporation
2026-07-08 · FDA_DEVICE
FDA Recall: Hillrom VOLARA System P.CIRCUIT 5KIT AC, (Single Patient Use Circuit), Model/Catalog Number REF M084
Baxter Healthcare Corporation
2026-07-08 · FDA_DEVICE
FDA Recall: Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circuit), Model/Catalog Number REF M08085; O
Baxter Healthcare Corporation
2026-07-08 · FDA_DEVICE
FDA Recall: Hillrom VOLARA System P.CIRCUIT KIT AC (Single Patient Use Circuit), Model/Catalog Number REF M08473
Baxter Healthcare Corporation