Target Detachable Coils: TARGET HELICAL NANO 1.5 MM X 2 CM MODEL Number:M0035431520 Neurol...
FDA Device Recall #Z-2169-2016 — Class II — June 6, 2016
Recall Summary
| Recall Number | Z-2169-2016 |
| Classification | Class II — Moderate risk |
| Date Initiated | June 6, 2016 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Stryker Neurovascular |
| Location | Fremont, CA |
| Product Type | Devices |
| Quantity | 45,302 (8,188 in the U.S.) - total, all model numbers |
Product Description
Target Detachable Coils: TARGET HELICAL NANO 1.5 MM X 2 CM MODEL Number:M0035431520 Neurology: Target Detachable Coils are intended to endovascularly obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels.
Reason for Recall
Stryker Neurovascular has become aware that some units of Target Nano product do not have the intended stretch resistance. The sutures inside the coil that provide stretch resistance may have been damaged during manufacturing which can lead to an increased occurrence of coil stretching.
Distribution Pattern
Worldwide Distribution - US (nationwide) and Australia, Austria, Belgium, Brazil, Bulgaria, Canada, Canary Islands, Chile, China, Colombia, Croatia, Czech Republic, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Ireland, Italia, Japan,Latvia, Lebanon, Libyan Arab Jamahiriya, Lithuania, Luxembourg, Mexico,Netherlands, Norway, Peru, Philippines, Poland, Portugal, Russia, Saudi Arabia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, and Vietnam.
Lot / Code Information
MODEL Number: M0035431520: Lot Number/Expiration Date: 18784673 31-Jan-19 18723226 30-Nov-18 18686302 30-Nov-18 18637332 31-Oct-18 18627687 31-Oct-18 18569824 31-Aug-18 18453278 30-Jun-18 18391505 31-May-18 18769932 31-Dec-18 18735994 30-Nov-18 18710356 30-Nov-18 18652851 31-Oct-18 18801847 31-Jan-19 18755945 31-Dec-18 18602481 30-Sep-18 18832966 28-Feb-19 18843005 28-Feb-19 18630099 31-Oct-18 18510994 31-Jul-18 18495363 31-Jul-18 18484141 31-Jul-18 18803162 31-Jan-19 18786297 31-Jan-19 18754879 31-Dec-18 18734778 30-Nov-18 18602423 30-Sep-18 18585290 31-Aug-18 18450430 30-Jun-18 18769816 31-Dec-18 18785485 31-Jan-19 18637274 31-Oct-18 18511110 31-Jul-18 18465901 30-Jun-18 18769700 31-Dec-18 18746995 31-Dec-18 18725103 30-Nov-18 18694228 30-Nov-18 18686012 30-Nov-18 18665561 31-Oct-18 18607752 30-Sep-18 18449575 30-Jun-18 18832355 28-Feb-19 18831744 31-Jan-19 18842138 28-Feb-19 18732878 30-Nov-18 18637216 31-Oct-18 18584252 31-Aug-18 18569882 31-Aug-18 18569766 31-Aug-18 18523410 31-Jul-18 19033487 30-Apr-19 18984845 30-Apr-19 18972140 30-Apr-19 18861952 28-Feb-19 18878607 28-Feb-19 19063170 31-May-19 18923191 31-Mar-19 18897527 28-Feb-19 18897185 28-Feb-19 18910290 31-Mar-19 19032199 30-Apr-19 19002213 30-Apr-19 19002155 30-Apr-19 18950942 31-Mar-19 18897698 28-Feb-19 18858983 28-Feb-19 19031329 30-Apr-19 19031909 30-Apr-19 19002271 30-Apr-19 18951058 31-Mar-19 18950884 31-Mar-19 18896843 28-Feb-19 18897014 28-Feb-19 18879010 28-Feb-19 18909942 31-Mar-19 18910638 31-Mar-19 18843872 28-Feb-19 19031619 30-Apr-19 19002329 30-Apr-19 18878204 28-Feb-19 18886556 28-Feb-19 18938172 31-Mar-19 18939594 31-Mar-19 18951000 31-Mar-19 18897356 28-Feb-19 18885142 28-Feb-19 18971589 30-Apr-19 18950826 31-Mar-19 18860449 28-Feb-19.
Other Recalls from Stryker Neurovascular
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-0021-2025 | Class II | The Trevo Trak 21 Microcatheter is a single-lum... | Aug 30, 2024 |
| Z-1903-2024 | Class II | Trevo ProVue, Catalog: 90184 | Apr 23, 2024 |
| Z-1908-2024 | Class II | DAC 044 115cm, Catalog: 90760 | Apr 23, 2024 |
| Z-1906-2024 | Class II | Trevo Trak 21 Microcatheter, Catalog: 90338 | Apr 23, 2024 |
| Z-1905-2024 | Class II | Trevo NXT ProVue 3 x 32, US, Catalog: 90312 ... | Apr 23, 2024 |
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.