Medtronic Handset with Communicator, Model TH90Q01, InterStim Smart Programmer and Communicator Kits, containing the Model HH90 Handset and the TM90 Communicator.
FDA Recall Z-3073-2024 · Posted 2024-09-06
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Recalling FirmMedtronic Neuromodulation
Recall StatusOpen, Classified
Product CodeEZW
Date Initiated2024-06-17
Product Quantity211 devices
Reason for Recall
A subset of the handsets within the kit may not be able to complete the pairing process with the communicator upon initial setup.
Firm 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.
Root Cause
Software change control
Distribution Pattern
US Nationwide distribution.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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