{"url_path":"/fda/device/recalls/Z-2066-2026","section_key":"summary","section_title":"DEVICE Recall: Windstone Medical Packaging, Inc. — Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes)    Angio Pack  Part numbers AMS6908E, AMS6908F","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-02","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2066-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Windstone Medical Packaging, Inc."},"word_count":132,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2066-2026\n\n**Recalling firm:** Windstone Medical Packaging, Inc.\n**Classification:** Class I\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-02\n**Report date:** 2026-05-20\n\n## Product\nCustom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes)    Angio Pack  Part numbers AMS6908E, AMS6908F\n\n## Reason\nAffected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose connection or full disconnection between syringe and manifold. If unwinding occurs, there is a potential for biohazard exposure, blood loss, infection. or air embolism.\n\n## Affected lots\nPack AMS6908E UDI-DI B098AMS6908E0 Lot 214875  Pack AMS6908F UDI-DI B098AMS6908F0 Lots 215436, 225001, 226706, 234088\n\n## Distribution\nUS Nationwide distribution in the state of Arizona."}