RECALL ALERT
Ongoing
XLSX-802EF0C494
Omnipod: Alternate controller enabled insulin infusion pump
Recalled by Insulet Corporation
Classification
—
Reason for Recall
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.
Product Details
Product Quantity
Not specified
Product Type
Food
Code Info
Not specified
Voluntary/Mandated
Not specified
Distribution & Geography
Distribution Pattern
Not specified
Company Location
Not specified
Timeline
Report Date
03/13/2026
Recall Initiated
03/13/2026
Classification Date
N/A
Termination Date
N/A
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 28, 2026
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