Home/Recalls/FDA-Z-1974-2026
FDA DevicesClass I

Halyard CATH LAB kit. Model Number: SACL75-01.

Published: May 13, 2026Recall ID: Z-1974-2026Category: devicesCountry: US

Reason for Recall / Hazard

Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Product Description & Identification

Halyard CATH LAB kit. Model Number: SACL75-01.

Additional Source Details

FieldValue
CityToano
StateVA
Event id98686
Address 19000 Westmont Dr
Code infoModel Number: SACL75-01. UDI (Kit Lot Numbers): (01)20809160481377(17)280520(10)341730(30)004(241)UINR44-01 (341730), (01)20809160481377(17)280623(10)341742(30)004(241)SACL75-01 (341742), (01)20809160481377(17)280609(10)345855(30)004(241)SACL75-01 (345855), (01)20809160481377(17)280609(10)345863(30)004(241)SACL75-01 (345863).
Postal code23168-9351
Report date20260513
Product typeDevices
Product quantity172 kits
Reason for recallPotential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260313
Initial firm notificationE-Mail
Center classification date20260501

Overview

  • Recalling FirmAVID Medical, Inc.
  • StatusOngoing
  • Risk LevelClass I
  • DistributionUS distribution to FL, IL, MO, MS, NC, NE, TX.
Official Agency Alert