FDA Device recall Z-2164-2016
Target Detachable Coils: TARGET 360 NANO 1.5 MM X 4 CM MODEL Number:M0035421540 Neurology: Target Detachable Coils are intended to endovasc…
- FDA Device
- Class II
- terminated
- Published 2016-07-20
On 2016-07-20 the FDA classified a Class II recall of Target Detachable Coils: TARGET 360 NANO 1.5 MM X 4 CM MODEL Number:M0035421540 Neurology: Target Detachable Coils are intended to endovasc… by Stryker Neurovascular, citing 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 resista….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2164-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-06-06 |
| Published | 2016-07-20 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker Neurovascular |
| Distribution | US |
Product
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
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.
Identifiers
| code_info | MODEL Number: M0035421540 Lot Number/Expiration Date: 18808912 31-Jan-19 18741434 31-Dec-18 18714072 30-Nov-18 1…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 18 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2164-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.