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Recall Observatory FDA recall evidence

Device product

Dekompressor Percutaneous Discectomy Probe. The Dekompressor is a single use disposable discectomy probe that passes through and works in conjunction with an introducer cannula to remove intervertebral disc nucleus pulposus material.

Z-0127-2014

November 04, 2013

Class II

Product summary

Firm
Stryker Instruments Div. of Stryker Corporation
Event
Event 66456
Status
Terminated
Classification
Class II
Quantity
20,385 total distributed since 2004
Official record key
device-enforcement:Z-0127-2014

Official wording

Reason: Stryker has identified a potential for the auger and/or cannula to fracture when the Dekompressor is used contrary to the warnings in the Instructions For Use (IFU). Specifically, manually bending the cannula can weaken the device and may result in a fracture of the auger and/or cannula. This could result in the need for additional medical intervention to remove the broken piece, pain or loss of m

Code information: Part Number(s) 0407-251-000, 0407-260-000, 0407-265-000, 0407-266-000, 0407-280-000, and 0407-281-000.

Distribution pattern: Nationwide Distribution including the states of AR, AZ, CA, CO, FL, GA, IL, KS, MS, ND, and NE.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Stryker has identified a potential for the auger and/or cannula to fracture when the Dekompressor is used contrary to the warnings in the Instructions For Use (IFU). Specifically, manually bending the cannula can weaken the device and may result in a fracture of the auger and/or cannula. This could result in the need for additional medical intervention to remove the broken piece, pain or loss of m