Official recall notice

FDA DeviceClass INotable

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

Recall date
2026-05-13
FDA class
Class I

Why it was recalled

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.

Recommended action

What to do

172 kits

Product description

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.

Verify with the official notice →
Share:

Related Recalls

2026-09-23 · FDA_DEVICE
FDA Recall: Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02;
AVID Medical, Inc.
2026-09-23 · FDA_DEVICE
FDA Recall: Halyard IV START KIT NON-STERILE REF: KRIV26-02
AVID Medical, Inc.
2026-09-23 · FDA_DEVICE
FDA Recall: Haylard UNIV IMAGING BIOPSY TRUCUSTOM; Model/Item Number (Kit): VARV042-03;
AVID Medical, Inc.
2026-09-23 · FDA_DEVICE
FDA Recall: Haylard CONTINUOUS NERVE BLOCK TRAY; Model/Item Number (Kit): BMCN001-05;
AVID Medical, Inc.