Home/Recalls/FDA-Z-1049-2026
FDA DevicesClass II

Medline Kits containing B. Braun IV Administration Sets and Pump Administration ...

Published: January 21, 2026Recall ID: Z-1049-2026Category: devicesCountry: US

Reason for Recall / Hazard

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

Product Description & Identification

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: AN01 CAROTID ANESTH KIT-LF, Medline Kit SKU PHS972096014B

Affected Products

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: AN01 CAROTID ANESTH KIT-LF, Medline Kit SKU PHS972096014B

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id98154
Address 13 Lakes Dr
Code infoUDI/DI 10889942695911 (EA) 40889942695912 (CA), Lot Numbers: 25JMC398
Postal code60093-2753
Report date20260121
Product typeDevices
Product quantity10 units
Reason for recallMedline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20251126
Initial firm notificationLetter
Center classification date20260112

Overview

  • Recalling FirmMedline Industries, LP
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution.
Official Agency Alert