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

Recall Z-2980-2020 — The Guardian Connect App CSS7200 iOS - Product Usage: intended for use by patients with a compatible consumer mobile device.

U.S. FDA — Device Enforcement · United States · 2020-07-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2980-2020
Date of alert
2020-07-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00763000255404
Reported risk: As a result of the release of new software version to CareLink Personal website, the IOS app for the Continuous Monitoring Glucose system stopped automatically uploading data to the website.
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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