Sutures, Non-absorbable, Steel, Monofilament and Multifilament, Sterile, Rx only, Product Usa...
FDA Device Recall #Z-1295-2014 — Class II — March 11, 2014
Recall Summary
| Recall Number | Z-1295-2014 |
| Classification | Class II — Moderate risk |
| Date Initiated | March 11, 2014 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Teleflex Medical |
| Location | Research Triangle Park, NC |
| Product Type | Devices |
| Quantity | Total 32,271 ea. |
Product Description
Sutures, Non-absorbable, Steel, Monofilament and Multifilament, Sterile, Rx only, Product Usage: A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or Ushaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.
Reason for Recall
The products are being recalled because they did not meet minimum needle attachment strength requirements.
Distribution Pattern
Worldwide Distribution - U.S. Nationwide and the countries of Canada, Germany, and Ireland
Lot / Code Information
Product Code: X-4981M4, Lot number: 02J0800451
Other Recalls from Teleflex Medical
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-0703-2020 | Class II | HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial ... | Oct 30, 2019 |
| Z-0688-2020 | Class II | Arrow EZ-IO Intraosseous Vascular Access System... | Oct 8, 2019 |
| Z-0689-2020 | Class II | Arrow EZ-IO Intraosseous Vascular Access System... | Oct 8, 2019 |
| Z-0690-2020 | Class II | Arrow EZ-IO Intraosseous Vascular Access System... | Oct 8, 2019 |
| Z-0496-2020 | Class II | WECK AutoEndo5, Automatic Hem-O-Lok Clip Applie... | Oct 4, 2019 |
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.