Home/Recalls/FDA-Z-2766-2026
FDA DevicesClass I

Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets

Published: August 19, 2026Recall ID: Z-2766-2026Category: devicesCountry: US
US
Medical DeviceFDA DevicesUSUS

Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets

Recalling Firm: Baxter Healthcare Corporation

Reason for Recall / 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.

Product Description & Identification

Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets

Additional Source Details

FieldValue
CityDeerfield
StateIL
Event id99343
Address 11 Baxter Pkwy
Code infoUDI/DI 00085412014319, Lot Numbers: DR26C27062, exp. 30-MAR-2028; DR26D14031, exp. 15-Apr-2028; DR26E13055, exp. 14-May-2028
Postal code60015-4625
Report date20260819
Product typeDevices
Product quantity24528 units
Reason for recallBaxter 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.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260630
Initial firm notificationLetter
Center classification date20260811

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Overview

  • Recalling FirmBaxter Healthcare Corporation
  • StatusOngoing
  • Risk LevelClass I
  • DistributionUS Nationwide. No OUS consignees.
Recall Hazard Severity
High Alert (Class I)
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