Home/Recalls/FDA-Z-2142-2026
FDA DevicesClass I

Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravasc...

Published: May 20, 2026Recall ID: Z-2142-2026Category: devicesCountry: US

Reason for Recall / Hazard

Medline has identified the presence of particulate within the fluid path of the Manifolds.

Product Description & Identification

Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravascular blood pressure transducer

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id98735
Address 13 Lakes Dr
Code infoUDI/DI each 10193489059205, UDI/DI case 30193489059209, Lot Numbers: 117277, 119982, 122210, 122199, 130129, 133014, 136396, 138613, 139138, 157974, 162399, 164317, 175538, 193515, 193531.
Postal code60093-2753
Report date20260520
Product typeDevices
Product quantity760 units
Reason for recallMedline has identified the presence of particulate within the fluid path of the Manifolds.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260324
Initial firm notificationTwo or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date20260508

Overview

  • Recalling FirmMedline Industries, LP
  • StatusOngoing
  • Risk LevelClass I
  • DistributionUS (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.
Official Agency Alert