FDA Recalls, Market Withdrawals & Safety AlertsOther / 其他

Alternate controller enabled insulin infusion pump

Recall fda-alert:2026-03-13:Omnipod:Alternate controller enabled insulin infusion pumpPublished 2026-03-13Company Insulet Corporation

Reason / 召回原因Pods may have a small tear in the internal tubing that delivers insulin. This may leak inside the Pod instead of being fully infused into the body as intended.

Distribution / 销售地区Not provided in the official record

Code information / 批次信息Not provided in the official record

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:2026-03-13:Omnipod:Alternate controller enabled insulin infusion pump

Classification / 风险等级

Other / 其他

Published / 发布时间

2026-03-13

Recalling firm / 召回企业

Insulet Corporation

Product description / 产品描述

Alternate controller enabled insulin infusion pump

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

Pods may have a small tear in the internal tubing that delivers insulin. This may leak inside the Pod instead of being fully infused into the body as intended.

Need the original notice?
Open the agency source for the complete official notice and any disposal, return, or contact instructions.

Open official source ↗

← Return to Recall Radar search / 返回搜索雷达

Last synchronized: 2026-03-13. Recall Radar does not replace agency guidance.