Class I
Medical Device Recall: Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model numbers ANCA80AP ANCA80AQ
American Contract Systems Inc · March 19, 2026
Reason for Recall
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.
Distribution
US distribution to MN. No OUS distribution.
States Affected
MN
Quantity Affected
7,311 kits
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1981-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.