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Recall Observatory FDA recall evidence

Device product

T8 REMOVAL HEAD, REF 8910641, QTY: 1 EA, Product Usage: The non-sterile T8 Removal Diriver is used with the Spire and Spire Z Spinal System in conjunction with the set screwdriver to remove the implant during removal surgery. The set screw driver is attached to the end of the removal head and used to disengage the remaining portion of the set screw within the device.

Z-2200-2013

August 12, 2013

Class II

Product summary

Firm
Medtronic Sofamor Danek USA Inc
Event
Event 66010
Status
Terminated
Classification
Class II
Quantity
9 units
Official record key
device-enforcement:Z-2200-2013

Official wording

Reason: One lot of the T8 Removal Head had incorrect hardness specification, which could result in the T8 Removal head failing during removal of the CD Horizon Spire and Spire Z Spinal System implant. There is a potential for tissue damage to occur and/or minor surgical delay to remove the remaining fragments of the tip.

Code information: RS12K008

Distribution pattern: USA Nationwide Distribution in the state of GA, AK, WA, and CA.

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    incorrect hardness specification