Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0437-2016 — MiniMed 620G, 3.0mL mg/dL, Model No. MMT-1710 The MiniMed 620G and MiniMed 640G insulin pump systems are indicated for the continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin. In addition, the pump system is indicated for

U.S. FDA — Device Enforcement · United States · 2015-09-25 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0437-2016
Date of alert: 2015-09-25
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Medtronic MiniMed Inc.
Product category: device
Product type: Devices

Reported risk: The pump drive motors may experience a malfunction which would result in a pump error message alarm notifying you that insulin is no longer being delivered. Possible cause is either lack of greasing or deficient greasing in a ball bearing assembly of the motor.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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