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Recall Observatory FDA recall evidence

Device product

MIRS for MATRIX Spine System. Minimally Invasive Reduction Screw (MIRS) for percutaneous instrumentation of the thoracolumbar spine. The Synthes USS are non-cervial spinal fixation devices intended for posterior pedicle screw fixation (T1-S2/ilium), posterior hook fixation (T1-L5), or anterolateral fixation (T8-L5).

Z-0001-2013

June 18, 2012

Class II

Product summary

Firm
Synthes USA HQ, Inc.
Event
Event 62773
Status
Terminated
Classification
Class II
Quantity
1602
Official record key
device-enforcement:Z-0001-2013

Official wording

Reason: Synthes is initiating a Medical Device Labeling Correction following a detailed review of the current labeling in response to reported complaints. Synthes has identified technique measures and has updated the labeling associated with this system. The labeling reflects updated technique recommendations and emphasizes the importance of avoiding rod mis-alignment.

Code information: Minimally Invasive Redution Screw System (MIRS) - Labeling number J11031-A

Distribution pattern: Nationwide Distribution including CA, FL, ID, IN, MD, MI, MT, LA, NY, OH, PA, TX, VA and WA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Synthes is initiating a Medical Device Labeling Correction following a detailed review of the current labeling in response to reported complaints. Synthes has identified technique measures and has updated the labeling associated with this system. The labeling reflects updated technique recommendations and emphasizes the importance of avoiding rod mis-alignment.