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Recall Observatory FDA recall evidence

Device product

P/N: 9735023, DRIVER 9735023 SOLERA 5.5/6.0 MAS; P/N: 9735024, DRIVER 9735024 SOLERA 5.5/6.0 MAS CAN; P/N: 9735025, DRIVER 9735025 SOLERA 5.5/6.0 RMAS; P/N: 9735026, DRIVER 9735026 SOLERA 5.5/6.0 RMAS CAN; P/N: 9735027,DRIVER 9735027 SOLERA 5.5/6.0 FAS/SAS. The Medtronic Navigated Solera Screwdrivers are reusable devices that are designed for use in spine surgery to assist in the placement of screws during the surgery, using a Medtronic computer-assisted surgery system.

Z-2823-2015

September 14, 2015

Class II

Product summary

Firm
Medtronic Navigation, Inc.
Event
Event 72183
Status
Terminated
Classification
Class II
Quantity
2,346
Official record key
device-enforcement:Z-2823-2015

Official wording

Reason: Specific use conditions can increase the possibility of a screwdriver tip deforming or breaking during surgery.

Code information: For this action, device lot numbers are not applicable. The action covers all lots of products distributed between September 2010 and July 2015

Distribution pattern: Worldwide Distribution - US (nationwide) and Internationally to Canada; United Arab Emirates; Australia; Belgium; Switzerland; China; Germany; Denmark; Spain; Finland; France; Great Britain; Greece; India; Israel; Italy; Japan; Netherlands; New Zealand; Poland; Portugal; Sweden; Singapore; Thailand; Slovakia; Turkey; and South Africa.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Specific use conditions can increase the possibility of a screwdriver tip deforming or breaking during surgery.