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Recall Observatory FDA recall evidence

Device product

OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected. Catalog Number(s): POD-ZXP420 (US). Intended for subcutaneous delivery of insulin at set and variable rates for the management of diabetes mellitus in persons requiring insulin.

Z-2484-2015

July 13, 2015

Class I

Product summary

Firm
Insulet Corporation
Event
Event 71651
Status
Terminated
Classification
Class I
Quantity
24829 boxes Expanded: 26,230.9 boxes
Official record key
device-enforcement:Z-2484-2015

Official wording

Reason: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to deploy/retract causing insulin to be pumped or the audible alarm is displayed on the PDM and pod will not deliver insulin

Code information: Lot Numbers: L40806, L40811, L40895, L40976, L41014, L41025, L41067, L41162, L41171, L41197, L41198, L41250 Expanded Recall: Lot Codes: L41880, L41881, L41892, L41895,L41897,L41898, L41899,L41900, L41901, L41902, L41903, L41904, L41905, L41906, L41907

Distribution pattern: Worldwide Distribution: US (Nationwide) and country of: Switzerland.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to deploy/retract causing insulin to be pumped or the audible alarm is displayed on the PDM and pod will not deliver insulin