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Recall Observatory FDA recall evidence

Device product

Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical instrument

Z-0914-2022

February 10, 2022

Class II

Product summary

Firm
Nextremity Solutions
Event
Event 89764
Status
Terminated
Classification
Class II
Quantity
239 units
Official record key
device-enforcement:Z-0914-2022

Official wording

Reason: Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery

Code information: Lot Number: 168A27917C UDI: 00817701020837

Distribution pattern: Distribution US Nationwide, Japan, and the Netherlands

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery

Field note

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