MIRS for MATRIX Spine System. Minimally Invasive Reduction Screw (MIRS) for percutaneous instrum...
FDA Device Recall #Z-0001-2013 — Class II — June 18, 2012
Recall Summary
| Recall Number | Z-0001-2013 |
| Classification | Class II — Moderate risk |
| Date Initiated | June 18, 2012 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Synthes USA HQ, Inc. |
| Location | West Chester, PA |
| Product Type | Devices |
| Quantity | 1602 |
Product Description
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).
Reason for Recall
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.
Distribution Pattern
Nationwide Distribution including CA, FL, ID, IN, MD, MI, MT, LA, NY, OH, PA, TX, VA and WA.
Lot / Code Information
Minimally Invasive Redution Screw System (MIRS) - Labeling number J11031-A
Other Recalls from Synthes USA HQ, Inc.
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-0393-2014 | Class II | Synthes Material Mix (Adjustable Cervical Distr... | Oct 15, 2013 |
| Z-0473-2014 | Class II | Synthes TomoFix Plates The Synthes J5606-C T... | Oct 9, 2013 |
| Z-0405-2014 | Class II | Synthes Implant Holder for Synfix (TM)-LR th... | Oct 8, 2013 |
| Z-0369-2014 | Class II | Synthes Titanium Trochanteric Fixation Nail (TF... | Oct 3, 2013 |
| Z-0394-2014 | Class II | Synthes Spiked Washers 13.5/6.5 Spiked Washe... | Oct 3, 2013 |
Frequently Asked Questions
Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.