Convenience kits containing Medline Namic Angiographic Control… — Class I medical device recall Z-1981-2026
Ongoing recall by American Contract Systems Inc, reported 2026-05-13, distributed in MN. Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use,
| Recall number | Z-1981-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | American Contract Systems Inc, Tiffin, OH, United States |
| Recall initiated | 2026-03-19 |
| Classified | 2026-05-06 |
| Reported by FDA | 2026-05-13 |
| Distributed | MN |
| Quantity | 7,311 kits |
| UPC / GTIN / UDI-DI | 00191072232168, 00191072236678 |
| Lot numbers | 42-8146111, 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, ANCA80AQ |
| Model numbers | ANCA80AP, ANCA80AQ |
Product
Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model numbers ANCA80AP ANCA80AQ
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1981-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.