Recall
FDAHealthMarch 19, 2026

American Contract Systems Inc — Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model numbers ANCA80AP ANCA80AQ

⚠️ 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.

Is this relevant to me?

Geography
US, MN
Source agency
FDA
Category
Health
Published
March 19, 2026

US distribution to MN. No OUS distribution.

What's affected?

Product
Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model numbers ANCA80AP ANCA80AQ
Lot code
42-8146111

Additional details

ANCA80AP UDI-DI 191072232168 Lot 42-8146111 ANCA80AQ UDI-DI 191072236678 Lots 42-8207211 42-8267711 42-8311311 42-8337611 42-8353311 42-8379211 42-8407111 42-8510711 42-8575111 42-8611511 42-8718911 42-8718912 42-8722611 42-8805311 42-8820611 42-8870911

What should I do?

Recommended action

Class I recall. Voluntary: Firm initiated Quantity affected: 7,311 kits.

View original FDA notice →

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