{"url_path":"/fda/device/recalls/Z-1981-2026","section_key":"summary","section_title":"DEVICE Recall: American Contract Systems Inc — Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor    CORONARY ANGIO PACK  Model numbers ANCA80AP  ANCA80AQ","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-03-19","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1981-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"American Contract Systems Inc"},"word_count":125,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-1981-2026\n\n**Recalling firm:** American Contract Systems Inc\n**Classification:** Class I\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-03-19\n**Report date:** 2026-05-13\n\n## Product\nConvenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor    CORONARY ANGIO PACK  Model numbers ANCA80AP  ANCA80AQ\n\n## Reason\nImpacted 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.\n\n## Affected lots\nANCA80AP 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\n\n## Distribution\nUS distribution to MN. No OUS distribution."}