FDA recall Z-1478-2024

Navinetics Inc · Class II · device

Product

NaviNetics Skull Anchor Key and Drill Kit, REF NN1215

Reason for recall

Defective Skull Anchor Key. After attachment of the single use Skull Anchor Key to the patient, the user was unable to attach the CT Localizer to perform stereotactic Imaging. Attachment of the localizer is typically accomplished by fully screwing in the four thumbscrews of the localizer into the threaded holes found on the top surface of the Skull Anchor Key.

Distribution

US Nationwide distribution in the states of FL, MN, CO.

Key facts

Status
Ongoing
Initiation date
2024-02-26
Report date
2024-04-10
Voluntary/Mandated
Voluntary: Firm initiated
Location
Rochester, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1478-2024