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FDA Medical Device Recalls (openFDA)

Medtronic Inc.: The Guardian Connect App CSS7200 iOS - Product Usage: intended for use by patients with a compatible consumer mobile device.

Recall number
Z-2980-2020
Recalling firm
Medtronic Inc.
Product
The Guardian Connect App CSS7200 iOS - Product Usage: intended for use by patients with a compatible consumer mobile device.
Status
Terminated
Initiated
2020-07-15
Posted
not on file
Terminated
2022-02-18
Reason
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.
Root cause
Software design
Action
On July 15, 2020, the firm sent an "URGENT FIELD SAFETY NOTIFICATION" to customers/Care Partners/Healthcare Professionals via email informing them that the Recalling Firm released an update to the CareLink Personal Software. Following the release of the software, several customer using the iOS app experienced data connectivity disruptions and as a result: 1. Care partners may not receive SMS alerts 2. Care partners remote access monitoring in the CareLink Connect web app may show data gaps 3. Customers may see data gaps in their reports. Customer are instructed to: 1. Attempt to manually upload your data to the CareLink" software via the Guardian" Connect app: a. Tap on the top left corner of the Home Screen b. Confirm Sync to CareLink is enabled c. Tap Upload Now d. Wait 10 minutes before moving to step #2. 2. Check your account to see if you are experiencing this issue a. From your mobile device visit https://carelink.minimed.eu and log in to your CareLink" account b. Confirm that your data is visible in the CareLink" Connect web app c. If your data is visible, no further action is needed - you are not experiencing the issue d. If your data is not visible, you may be experiencing the issue and you should complete the steps in the next section to resolve the issue. Instructions for Resolving the Issue (refer to the Frequently Asked Questions included for detailed instructions) 1. If your data was not visible after step #2, uninstall the Guardian" Connect app from your mobile device. For help, please refer to FAQ below #3 2. Unpair your transmitter from your mobile device. For help, please refer to FAQ below #3 3. Re-install the Guardian" Connect app on your mobile device this will restore the CareLink" connection. For help, please refer to FAQ below #4 *Uninstalling the Guardian" Connect app may delete visible data from the app. All data that has been uploaded to the CareLink" software will continue to be visible in CareLink" report
Quantity
3,588 users
Distribution
International distribution including in the countries of EMEA - Austria, Belgium, Croatia, Czechia, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Israel, Italy, Kuwait, Latvia, Luxembourg, The Netherlands, Poland, Portugal, Romania, Saudi Arabia, Serbia, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Turkey, Ukraine, United Arab Emirates, and United Kingdom. Latin America- Chile, Colombia and Mexico Asia Pacific (APAC) - Australia, India, Japan, The Republic of Korea, Malaysia, New Zealand, Russia Federation, Singapore, Thailand, and Vietnam. Asia - Hong Kong North America - Canada
Lot, serial or model codes
Product Number - CSS7200 UDI (GTIN.UPN) - 00763000255404
510(k) numbers
not on file
PMA numbers
not on file
Product code
MDS
Firm FEI
3003166194
Firm city
Northridge
Firm state
CA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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