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

Recall Z-0956-2020 — Medtronic MiniMed 670G System with SmartGuard, Ref #s/Model Number(s) - MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762, MMT-1580, MMT-1581, MMT-1582, MMT-1780, MMT-1781, and MMT-1782

U.S. FDA — Device Enforcement · United States · 2019-11-21 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0956-2020
Date of alert
2019-11-21
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Medtronic Inc.
Product category
device
Product type
Devices
Reported risk: There have been reported incidents of a loose reservoir that can no longer be locked into the pump. The reservoir can become loose due to a broken or missing retainer ring that prevents a proper lock. If the reservoir is not properly locked into the pump, it could lead to over or under delivery of insulin, which could then result in hypoglycemia or hyperglycemia.
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.

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