Target Detachable Coils: TARGET 360 NANO 3MM X 6CM MODEL Number:M0035443060 Neurology: Tar...
FDA Device Recall #Z-2176-2016 — Class II — June 6, 2016
Recall Summary
| Recall Number | Z-2176-2016 |
| 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 360 NANO 3MM X 6CM MODEL Number:M0035443060 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: M0035443060: Lot Number/Expiration Date: 18826753 31-Jan-19 18826606 31-Jan-19 18794421 31-Jan-19 18777349 31-Dec-18 18750808 31-Dec-18 18754448 31-Dec-18 18760112 31-Dec-18 18491003 31-Jul-18 18443198 30-Jun-18 18827047 31-Jan-19 18816704 31-Jan-19 18776301 31-Dec-18 18750603 31-Dec-18 18491065 31-Jul-18 18442058 30-Jun-18 18808498 31-Jan-19 18783540 31-Jan-19 18764659 31-Dec-18 18750193 31-Dec-18 18708724 30-Nov-18 18491096 31-Jul-18 18443258 30-Jun-18 18443228 30-Jun-18 18393950 31-May-18 18817367 31-Jan-19 18782584 31-Jan-19 18755514 31-Dec-18 18703469 30-Nov-18 18443018 30-Jun-18 18442958 30-Jun-18 18442538 30-Jun-18 18441728 30-Jun-18 18436622 30-Jun-18 18827341 31-Jan-19 18809086 31-Jan-19 18809674 31-Jan-19 18765615 31-Dec-18 18750398 31-Dec-18 18471007 31-Jul-18 18490724 31-Jul-18 18818030 31-Jan-19 18760113 31-Dec-18 18708786 30-Nov-18 18490972 31-Jul-18 18442508 30-Jun-18 18442268 30-Jun-18 18827194 31-Jan-19 18703264 30-Nov-18 18490910 31-Jul-18 18442568 30-Jun-18 18827488 31-Jan-19 18826900 31-Jan-19 18808792 31-Jan-19 18443048 30-Jun-18 19013252 30-Apr-19 19000510 30-Apr-19 18951824 31-Mar-19 18853836 28-Feb-19 19028176 30-Apr-19 18990655 30-Apr-19 19041022 31-May-19 19040295 31-May-19 19000572 30-Apr-19 18960708 31-Mar-19 18902391 28-Feb-19 19013163 30-Apr-19 19066272 31-May-19 19063700 31-May-19 18975258 30-Apr-19 18974821 30-Apr-19 18905927 31-Mar-19 19028296 30-Apr-19 19013074 30-Apr-19 18952060 31-Mar-19 18951116 31-Mar-19 18905896 28-Feb-19 18901749 28-Feb-19 18990624 30-Apr-19 18952296 31-Mar-19 19028056 30-Apr-19 19012985 30-Apr-19 18975695 30-Apr-19 18943458 31-Mar-19 18926529 31-Mar-19 18903033 28-Feb-19 19027936 30-Apr-19 19039567 31-May-19 19000541 30-Apr-19 18960301 31-Mar-19 18951588 31-Mar-19 18943981 31-Mar-19 18883033 28-Feb-19 18925429 31-Mar-19 18944504 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.