Target Detachable Coils: TARGET HELICAL NANO 1.5 MM X 3 CM MODEL Number:M0035431530 Neurol...
FDA Device Recall #Z-2170-2016 — Class II — June 6, 2016
Recall Summary
| Recall Number | Z-2170-2016 |
| 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 3 CM MODEL Number:M0035431530 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: M0035431530: Lot Number/Expiration Date: 18758254 31-Dec-18 18685258 30-Nov-18 18651285 31-Oct-18 18637564 31-Oct-18 18426876 31-May-18 18802748 31-Jan-19 18758459 31-Dec-18 18709486 30-Nov-18 18637506 31-Oct-18 18551662 31-Aug-18 18551894 31-Aug-18 18551778 31-Aug-18 18503529 31-Jul-18 18466471 30-Jun-18 18841964 31-Jan-19 18829601 31-Jan-19 18758049 31-Dec-18 18767569 31-Dec-18 18685548 30-Nov-18 18651227 31-Oct-18 18551604 31-Aug-18 18830630 31-Jan-19 18843698 28-Feb-19 18842831 31-Jan-19 18637390 31-Oct-18 18592500 30-Sep-18 18557240 31-Aug-18 18627281 31-Oct-18 18776363 31-Dec-18 18767070 31-Dec-18 18732530 30-Nov-18 18551836 31-Aug-18 18453506 30-Jun-18 18815140 31-Jan-19 18814270 31-Jan-19 18780961 31-Jan-19 18766571 31-Dec-18 18637448 31-Oct-18 18522949 31-Jul-18 18518477 31-Jul-18 18801433 31-Jan-19 18777411 31-Dec-18 18735646 31-Dec-18 18734430 30-Nov-18 18685838 31-Oct-18 18722263 30-Nov-18 18458818 30-Jun-18 18402198 31-May-18 19049471 31-May-19 19005345 30-Apr-19 18975463 30-Apr-19 18895272 28-Feb-19 18985193 30-Apr-19 19005403 30-Apr-19 19060071 31-May-19 18974589 30-Apr-19 18944128 31-Mar-19 18943082 31-Mar-19 19032025 30-Apr-19 18950234 31-Mar-19 18862184 28-Feb-19 18860682 28-Feb-19 18877220 28-Feb-19 19031155 30-Apr-19 18949886 31-Mar-19 18949712 31-Mar-19 18896142 28-Feb-19 18895852 28-Feb-19 18859219 28-Feb-19 18889081 28-Feb-19 19031445 30-Apr-19 18928887 31-Mar-19 18928128 31-Mar-19 19005287 30-Apr-19 18974152 30-Apr-19 18950060 31-Mar-19 18944651 31-Mar-19 18888559 28-Feb-19 19031735 30-Apr-19 19050513 31-May-19 18975026 30-Apr-19 18888037 28-Feb-19 18943605 31-Mar-19 18927369 31-Mar-19 18894982 28-Feb-19 18876352 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.