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

Recall Z-0516-2021 — MiniMed 670G, insulin pump, Ref/Model # MMT-1760KPK, MMT-1762KCN, MMT-1762WWK - Product Usage: indicated for continuous or periodic monitoring of glucose levels in the fluid under the skin, and detecting possible low and high glucose episodes. When using a sensor and transmitter, the pump displays c

U.S. FDA — Device Enforcement · United States · 2020-04-30 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0516-2021
Date of alert: 2020-04-30
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Medtronic Inc.
Product category: device
Product type: Devices

Reported risk: Missing solder battery connection, which could interrupt power of insulin pump.

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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