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Terminated

Animas Vibe Insulin Infusion Pump. This product is indicated for continuous subcutaneous infusion of insulin for the treatment of diabetes and has a continuous glucose monitoring feature.

FDA Recall Z-1034-2015 · Posted 2015-01-30

Recalling FirmAnimas Corporation
Recall StatusTerminated
Product CodeOYC
Date Initiated2011-09-06
Date Terminated2015-08-10
Product Quantity1235

Reason for Recall

Calibration factors in the pump overwritten during a programming step. The force sensor could send a lower signal value to the pump processor, with loss of prime warnings, occlusion alarms and the pump unable to detect a cartridge during the prime sequence. Field action initiated 8/29/2011.

Firm Action

The field action was initiated on 8/29/2011 and comprised communication to patients and distributors using email, letters and verbal communication. In addition, notifications were sent to those Health Care Professionals who had patients that were affected by this field action. Health Authorities were notified in those countries where the pump had been distributed (France, Germany, Sweden and United Kingdom) or was in the hands of patients. Replacement product was provided to distributors and end users who were identified as having affected product.

Root Cause

Software design (manufacturing process)

Distribution Pattern

No US distribution, Distributors are located in France, Germany, Sweden and United Kingdom.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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