AVID Medical, Inc. recalls Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.

Recall date

March 13, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1979-2026

FDA classification

Class I

Brand / firm

AVID Medical, Inc.

Sold / distributed

US distribution to FL, IL, MO, MS, NC, NE, TX.

Why it was recalled

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.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.