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Recall Observatory FDA recall evidence

Device product

Neurostimulation Kit (Ported, Dual 8, 40 cm), REF: 71005-US Peripheral Nerve Stimulation Kit (Ported, Dual 8, 40 cm), REF: 71019-US Components of the Nalu Spinal Cord Stimulation System.

Z-2257-2024

June 03, 2024

Class II

Product summary

Firm
Nalu Medical, Inc.
Event
Event 94682
Status
Ongoing
Classification
Class II
Quantity
13
Official record key
device-enforcement:Z-2257-2024

Official wording

Reason: Neurostimulation Systems have a manufacturing non-conformance that may reduce the efficiency of the radiofrequency signals between the Implantable Pulse Generator (IPG) and the Therapy Disc, causing the IPG to be non-functional, which causes the device to be non-functional so it will no longer inhibit the transmission of pain signals to the brain.

Code information: UDI-DI: 71005-US: 00812537036137, 00812537033600, 00812537033518, 00812537030975, 00812537030524. 71019-US: 00812537036441, 00812537035604, 00812537035598 Serial Numbers: H01377, H01382, H01432, H01419, H01387, H01445, H01415, H01441, H01373, H01428, H01378, H01438, H01431

Distribution pattern: US Nationwide distribution in the states of MO, IL, CA, TX, TN, OK, AZ, AR.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Neurostimulation Systems have a manufacturing non-conformance that may reduce the efficiency of the radiofrequency signals between the Implantable Pulse Generator (IPG) and the Therapy Disc, causing the IPG to be non-functional, which causes the device to be non-functional so it will no longer inhibit the transmission of pain signals to the brain.