Home/Recalls/FDA-Z-2141-2026
FDA DevicesClass I

Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107; Extravasc...

Published: May 20, 2026Recall ID: Z-2141-2026Category: 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 64037107; Extravascular blood pressure transducer

Additional Source Details

FieldValue
CityNorthfield
StateIL
Event id98735
Address 13 Lakes Dr
Code infoUDI/DI each 10193489059137, UDI/DI case 30193489059131, Lot Numbers: 89181, 95326, 95254, 102287, 102286, 102706, 105362, 105558, 108608, 112242, 112243, 115437, 118477, 121180, 121645, 122708, 126024, 131603, 136583, 140860, 142371, 146728, 147474, 148571, 152020, 153175, 163216, 175580, 176810, 184394, 191388, 193141.
Postal code60093-2753
Report date20260520
Product typeDevices
Product quantity6390 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