Target Detachable Coils: TARGET HELICAL NANO 1 MM X 3 CM MODEL Number:M0035431030 Neurol...
FDA Device Recall #Z-2167-2016 — Class II — June 6, 2016
Recall Summary
| Recall Number | Z-2167-2016 |
| 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 MM X 3 CM MODEL Number:M0035431030 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: M0035431030; Lot Number/Expiration Date: 18801491 31-Jan-19 18757273 31-Dec-18 18709428 30-Nov-18 18602133 30-Sep-18 18523870 31-Jul-18 18802806 31-Jan-19 18664601 31-Oct-18 18569137 31-Aug-18 18517839 31-Jul-18 18486090 31-Jul-18 18842022 31-Jan-19 18651923 31-Oct-18 18651865 31-Oct-18 18607288 30-Sep-18 18518071 31-Jul-18 18774611 31-Dec-18 18762227 31-Dec-18 18637042 31-Oct-18 18564861 31-Aug-18 18843756 28-Feb-19 18842889 31-Jan-19 18781019 31-Jan-19 18651981 31-Oct-18 18546861 31-Aug-18 18447942 30-Jun-18 18830688 31-Jan-19 18815198 31-Jan-19 18814328 31-Jan-19 18736978 30-Nov-18 18592210 30-Sep-18 18517955 31-Jul-18 18414488 31-May-18 18829659 31-Jan-19 18583312 31-Aug-18 18984903 30-Apr-19 19050397 31-May-19 18883354 28-Feb-19 18911821 31-Mar-19 19041285 30-Apr-19 18944244 31-Mar-19 18922785 31-Mar-19 18902333 28-Feb-19 18911418 31-Mar-19 18857263 28-Feb-19 18973207 30-Apr-19 19041807 30-Apr-19 19065916 31-May-19 19063344 31-May-19 18901691 28-Feb-19 19074243 31-May-19 19049355 31-May-19 19042329 31-May-19 19005113 30-Apr-19 18944767 31-Mar-19 18973553 30-Apr-19 18943198 31-Mar-19 18943721 31-Mar-19 19042851 31-May-19 18855184 28-Feb-19 19048313 31-May-19 18972861 30-Apr-19 18953849 31-Mar-19 18912224 31-Mar-19 19005171 30-Apr-19 18902975 28-Feb-19 18912627 31-Mar-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.