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Target Detachable Coils: TARGET 360 NANO 1.5 MM X 4 CM MODEL Number:M0035421540 Neurology: T...

FDA Device Recall #Z-2164-2016 — Class II — June 6, 2016

Recall Summary

Recall Number Z-2164-2016
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 1.5 MM X 4 CM MODEL Number:M0035421540 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: M0035421540 Lot Number/Expiration Date: 18808912 31-Jan-19 18741434 31-Dec-18 18714072 30-Nov-18 18677229 30-Nov-18 18625483 31-Oct-18 18625541 31-Oct-18 18642784 31-Oct-18 18633921 31-Oct-18 18598299 30-Sep-18 18590470 30-Sep-18 18542363 31-Aug-18 18420011 31-May-18 18419897 31-May-18 18833256 28-Feb-19 18808618 31-Jan-19 18787244 31-Jan-19 18677171 30-Nov-18 18524564 31-Jul-18 18524622 31-Jul-18 18832645 31-Jan-19 18768683 31-Dec-18 18756119 31-Dec-18 18725503 30-Nov-18 18666721 31-Oct-18 18642842 31-Oct-18 18642668 31-Oct-18 18598183 30-Sep-18 18590528 30-Sep-18 18578953 30-Sep-18 18406806 31-May-18 18809794 31-Jan-19 18787859 31-Jan-19 18755053 31-Dec-18 18741144 31-Dec-18 18701144 30-Nov-18 18590586 30-Sep-18 18579069 30-Sep-18 18549270 31-Aug-18 18420182 31-May-18 18420239 31-May-18 18809206 31-Jan-19 18817972 28-Feb-19 18701318 30-Nov-18 18677113 30-Nov-18 18488340 31-Jul-18 18598125 30-Sep-18 18542305 31-Aug-18 18787449 31-Jan-19 18714246 30-Nov-18 18625599 31-Oct-18 18634037 31-Oct-18 18598241 30-Sep-18 18559192 31-Aug-18 18832034 31-Jan-19 18817309 28-Feb-19 18787654 31-Jan-19 18768041 31-Dec-18 18701260 30-Nov-18 18809500 31-Jan-19 18701202 30-Nov-18 18677287 30-Nov-18 18642726 31-Oct-18 18590412 30-Sep-18 18559250 31-Aug-18 19080127 31-May-19 19010580 30-Apr-19 18931017 31-Mar-19 18885811 28-Feb-19 18846227 28-Feb-19 19026877 30-Apr-19 19025829 30-Apr-19 19043083 31-May-19 18974705 30-Apr-19 18957691 31-Mar-19 18911592 31-Mar-19 18845848 28-Feb-19 19049933 31-May-19 18998580 30-Apr-19 18853712 28-Feb-19 18887225 28-Feb-19 19080305 31-May-19 19026353 30-Apr-19 18998638 30-Apr-19 18975142 30-Apr-19 18956531 31-Mar-19 19079949 31-May-19 18964774 31-Mar-19 19042039 30-Apr-19 19010180 30-Apr-19 18963382 31-Mar-19 18912801 31-Mar-19 18911995 31-Mar-19 18846606 28-Feb-19 18963846 31-Mar-19 18930672 31-Mar-19 18899164 28-Feb-19 18912398 31-Mar-19 18974268 30-Apr-19 18987031 30-Apr-19 19050975 31-May-19 19048891 31-May-19 19042561 31-May-19 19041517 30-Apr-19 18964310 31-Mar-19 18975579 30-Apr-19 18957111 31-Mar-19 18940339 31-Mar-19 18938917 31-Mar-19 18929982 31-Mar-19 18845469 28-Feb-19.

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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.

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