Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating… Recall
Issued May 13, 2026 · American Contract Systems Inc
In May 2026, American Contract Systems Inc recalled the Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact American Contract Systems Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Recall details
- Brand
- American Contract Systems Inc
- Category
- Health
- Recall date
- May 13, 2026
- Units affected
- Not reported
- Sold at
- US distribution to MN. No OUS distribution.
- Recall number
- FDA-Z-1981-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- American Contract Systems Inc has 11 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.