Home/Recalls/FDA-Z-1973-2026
FDA DevicesClass I

Halyard CATH LAB kit. Model Number: SACL75AM.

Published: May 13, 2026Recall ID: Z-1973-2026Category: 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: SACL75AM.

Additional Source Details

FieldValue
CityToano
StateVA
Event id98686
Address 19000 Westmont Dr
Code infoModel Number: SACL75AM. UDI-DI (Kit Lot Numbers): 10809160413586 (1599684, 1601393).
Postal code23168-9351
Report date20260513
Product typeDevices
Product quantity228 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