Recall Z-0178-2020

Medtronic Inc. · initiated August 7, 2018

Class I Terminated

Class I – dangerous or defective products that could cause serious health problems or death

Product

Minimed Model 503 Remote Transmitter (MMT-503, MMT-503EU, MMT-503NA, MMT-503US) for use with the MiniMed Paradigm Insulin Pump (MMT-523/723, MMT-523K/723K, MMT-551/751, MMT-554/754, MMT-522/722, MMT-522K/722K, MMT-515/715, MMT-512/712, MMT-511)

Codes / lots: All serial numbers

Reason for recall

There is a potential security vulnerability related to the use of the remote controller accessories with the insulin pumps.

FDA-determined cause: Software design

Action taken

Medtronic sent an Urgent Field Safety Notification letter dated August 7, 2018 to the patient, distributor, and healthcare provider via email, U.S. mail, or phone. The letter identified the affected product, problem and actions to be taken. Starting on 10/05/2021, recall notices were sent to patients, health care professionals, distributors, and personnel at clinical sites. Distributors were asked to provide their customer lists to the recalling firm so the recalling firm could send customers recall notices. The scope of the recall is being expanded to all users regardless of warranty status. Users are asked to stop using and disconnect the remote controller, disable the remote feature, and return the remote controller to the recalling firm. Customers were also asked to provide the information requested in the confirmation form to the recalling firm via phone, mail, email, or online on the firm's website. Additional questions can be directed to Technical Support at 1-800-378-2292. Disconnecting/Disabling instructions were provided in the recall notice, which provided the following link: https://info.medtronicdiabetes.com/remote-controller-return

Details

Recall number
Z-0178-2020
Initiated
August 7, 2018
Posted by FDA
November 4, 2019
Terminated
March 29, 2024
Product code
LZG – Pump, Infusion, Insulin
Quantity
141,519
Distribution
Distribution was nationwide to consumers and distributors. There was no government/military distribution. Foreign distribution was made to Algeria, Australia, Austria, Belgium, Brazil, Canada, China, Croatia, Czech Republic, Denmark, Estonia, Faroe Islands, Finland, France, Germany, Greece, Hungary, Iceland, India, Iran, Iraq, Ireland, Israel, Italy, Kuwait, Latvia, Lebanon, Lithuania…
Recalling firm
Medtronic Inc., Northridge, CA

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0177-2020 Class IMinimed Model 500 Remote Control (MMT-500, MMT-500RU, MMT-500RUS, MMT-500RSE…There is a potential security vulnerability related to the use of the remote controller accessories with the… 08/07/2018Terminated