American Contract Systems Inc recalls Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model…

Recall date

March 19, 2026

Source

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

Recall number

Z-1981-2026

FDA classification

Class I

Brand / firm

American Contract Systems Inc

Sold / distributed

US distribution to MN. No OUS distribution.

Why it was recalled

Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full disconnection between the syringe and manifold. Potential risk for biohazard exposure, blood loss, infection, or air embolism.

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

Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model numbers ANCA80AP ANCA80AQ