FDA Device recall Z-2160-2016
Target Detachable Coils: TARGET 360 NANO 1 MM X 2 CM MODEL Number: M0035421020 Neurology: Target Detachable Coils are intended to endovascu…
- 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 MM X 2 CM MODEL Number: M0035421020 Neurology: Target Detachable Coils are intended to endovascu… 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-2160-2016 |
| 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 MM X 2 CM MODEL Number: M0035421020 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: M0035421020: Lot Number/Expiration Date: 18825272 31-Jan-19 18811666 31-Jan-19 18819711 31-Jan-19 18…MODEL Number: M0035421020: Lot Number/Expiration Date: 18825272 31-Jan-19 18811666 31-Jan-19 18819711 31-Jan-19 18790659 31-Jan-19 18701550 30-Nov-18 18628881 31-Oct-18 18598937 30-Sep-18 18562915 31-Aug-18 18582507 30-Sep-18 18582275 31-Aug-18 18819885 31-Jan-19 18811840 31-Jan-19 18742370 30-Nov-18 18714594 30-Nov-18 18723922 30-Nov-18 18701782 30-Nov-18 18701608 30-Nov-18 18677925 30-Nov-18 18657200 31-Oct-18 18667185 31-Oct-18 18667069 31-Oct-18 18647521 31-Oct-18 18599227 30-Sep-18 18582565 30-Sep-18 18553961 31-Aug-18 18790775 31-Jan-19 18790543 31-Jan-19 18742602 31-Dec-18 18647347 31-Oct-18 18604218 30-Sep-18 18585521 31-Aug-18 18515100 31-Jul-18 18825330 31-Jan-19 18790717 31-Jan-19 18723864 30-Nov-18 18742428 31-Dec-18 18714478 30-Nov-18 18729520 30-Nov-18 18677693 30-Nov-18 18657142 31-Oct-18 18638318 31-Oct-18 18647405 31-Oct-18 18604160 30-Sep-18 18825156 31-Jan-19 18825214 31-Jan-19 18819827 31-Jan-19 18811724 31-Jan-19 187 |
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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-2160-2016%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.