FDA Recall Open, Classified

Medtronic Handset with Communicator, Model TH90Q01, InterStim Smart Programmer and Communicator Kits, containing the Model HH90 Handset and the TM90 Communicator.

Recall: Z-3073-2024 · Initiated June 17, 2024

Recall

Recall Number
Z-3073-2024
Event Number
95131
Firm
Medtronic Neuromodulation
FEI Number
2182207
Product Code
EZW
Status
Open, Classified
Root Cause
Software change control
Initiated
June 17, 2024
Posted
September 6, 2024
Address
7000 Central Ave Ne, Minneapolis, MN, 55432-3568

Description

Medtronic Handset with Communicator, Model TH90Q01, InterStim Smart Programmer and Communicator Kits, containing the Model HH90 Handset and the TM90 Communicator.

Reason

A subset of the handsets within the kit may not be able to complete the pairing process with the communicator upon initial setup.

Action

The recalling firm issued letters dated June 2024 beginning 6/17/2024 to the Medtronic Field Service Representatives to notify consignees and retrieve a subset of the InterStim Smart Programmer and Communicator Kits (TH90Q01). The notification informed the Field Service Representatives of the Field Corrective Action and provided instruction on notifying the consignees and retrieving the device(s). Beginning on June 17, 2024, US initiated communications and notifications dated June 2024 were physically hand-delivered to each consignee with the impacted device(s). The letter described the issue and provided Required Customer Actions, which included completing and signing the Customer Confirmation form acknowledging receipt of the notification and sharing the notice with all that needed to be aware. An appendix was enclosed which listed the serial numbers of the affected products.

Distribution

US Nationwide distribution.

Quantity

211 devices