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Recall Observatory FDA recall evidence

Device product

VariSoft infusion set, Model Number 1002830

Z-0234-2024

October 11, 2023

Class I

Product summary

Firm
Unomedical A/S
Event
Event 93269
Status
Ongoing
Classification
Class I
Quantity
3362 units
Official record key
device-enforcement:Z-0234-2024

Official wording

Reason: The Varisoft infusion set is used in conjunction with tandem insulin pumps. The defect reported was damage to the connector piece during manufacturing. This damage results in the connector becoming detached more easily from the insulin set than expected, requiring less force to disconnect than intended. Disconnection, when not detected, for example during sleep, leads to missed basal dosing. which in turn can result in elevated blood glucose and ketone level (nocturnal hyperglycemia). Diabetic ketoacidosis.

Code information: GTIN 05705244018792, Serial Numbers: 5388368; GTIN 05705244018785, Serial Numbers: 5388368

Distribution pattern: US Nationwide distribution in the state of CA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The Varisoft infusion set is used in conjunction with tandem insulin pumps. The defect reported was damage to the connector piece during manufacturing. This damage results in the connector becoming detached more easily from the insulin set than expected, requiring less force to disconnect than intended. Disconnection, when not detected, for example during sleep, leads to missed basal dosing. which in turn can result in elevated blood glucose and ketone level (nocturnal hyperglycemia). Diabetic ketoacidosis.