Multi Vector Distractor Pin Holding Clamp, limited bone stock The holding clamp is part of the...
FDA Device Recall #Z-1745-2013 — Class II — May 31, 2013
Recall Summary
| Recall Number | Z-1745-2013 |
| Classification | Class II — Moderate risk |
| Date Initiated | May 31, 2013 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Synthes USA HQ, Inc. |
| Location | West Chester, PA |
| Product Type | Devices |
| Quantity | 121 |
Product Description
Multi Vector Distractor Pin Holding Clamp, limited bone stock The holding clamp is part of the Multi Vector Distractor which cis used for mandibular bone lengthening, including conditions such as congenital mandibular deficiencies or post-traumatic defects. The Multi Vector Distractor can be utilized to perform bone transport procedures as an alternative to bone grafts and free flaps.
Reason for Recall
Synthes is initiating a voluntary Medical Device removal for specified part numbers and lot numbers of the Mutis Vector Distractor Pin Holding clamp, limited bone stock. The firm received complaints that the clamp and nut construct would not engage the distractor arm threads and subsequently bind. It is not likely that a serious adverse event will result due to a nonconforming clamp, however there
Distribution Pattern
US Nationwide Distribution including the states of MA, TX, MN, SC, UT, VA, and NY.
Lot / Code Information
Titanium Multi Vector Distractor Pin Holding Clamp, body, limited bone stock Part # 487.941 with lot numbers: 3769720, 3779569, 3788731, 3794434, 7806093, 7823463 and Titanium Multi Vector Distractor Pin Holding Clamp, ramus, limited bone stock Part # 487.942 with lot numbers: 3769706, 3779571, 3788741, 7806096, 7823464.
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.