American Contract Systems recalls convenience kits with Medline Namic Angiographic Control Syringes that may disconnect during use, risking blood exposure, infection, or air embolism. Affected kits have specific model numbers and lots.
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.
American Contract Systems is recalling convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptors. The syringes may disconnect during use, potentially causing blood exposure, infection, or air embolism. Affected kits have specific model numbers and production lots.
The rotating adaptor on the syringe may unwind during use, causing a loose or full disconnection between the syringe and manifold. This disconnection can lead to biohazard exposure, blood loss, infection, or air embolism.
Healthcare professionals using these kits for coronary angiography procedures are most at risk. Patients receiving procedures with these kits could also be affected.
Check for model numbers ANCA80AP or ANCA80AQ with specific production lots listed in the recall notice. The kits are sold under the brand name American Contract Systems.
Immediately stop using the recalled convenience kits if you have them.
Affected model numbers are ANCA80AP and ANCA80AQ with specific production lots listed in the recall notice.
The rotating adaptor may unwind during use, causing a loose or full disconnection that could lead to blood exposure, infection, or air embolism.
Check the model numbers and production lots listed in the recall notice: ANCA80AP or ANCA80AQ with specific lots like 42-8146111.
We’ve drafted a message you can send American Contract Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-1981-2026 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1981-2026 from American Contract Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
