Angio Packs (AMS6908E and AMS6908F)
Official-information notice / 官方信息说明
This page organizes fields from the named agency record. It is not medical, legal, or food-safety advice. Always compare your package with the official notice.
Official record details
官方记录详情：以原始机构公告为准
Recall number / 召回编号
fda-alert:2026-04-20:Aligned Medical Angio Pack:Angio Packs (AMS6908E and AMS6908F)
Classification / 风险等级
Other / 其他
Published / 发布时间
2026-04-20
Recalling firm / 召回企业
Windstone Medical Packaging dba Aligned Medical Solutions
Product description / 产品描述
Angio Packs (AMS6908E and AMS6908F)
Product code / 产品代码
Not provided in the official record
Code information / 批次与代码信息
Not provided in the official record
Product quantity / 产品数量
Not provided in the official record
Distribution / 销售地区
Not provided in the official record
Reason for recall / 召回原因
Risk of the syringe rotating adapter unwinding during use, which may result in a loose connection and/or full disconnection between the syringes and manifold, potentially causing biohazard exposure, blood loss, infection, or air embolism.
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Last synchronized: 2026-04-20. Recall Radar does not replace agency guidance.