FDA Device recall Z-2163-2016
Target Detachable Coils: TARGET 360 NANO 1.5 MM X 3 CM MODEL Number: M0035421530 Neurology: Target Detachable Coils are intended to endovas…
- 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 3 CM MODEL Number: M0035421530 Neurology: Target Detachable Coils are intended to endovas… 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-2163-2016 |
| 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 3 CM MODEL Number: M0035421530 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: M0035421530 Lot Number/Expiration Date: 18576579 31-Aug-18 18825794 31-Jan-19 18759372 31-Dec-18 1…MODEL Number: M0035421530 Lot Number/Expiration Date: 18576579 31-Aug-18 18825794 31-Jan-19 18759372 31-Dec-18 18769642 31-Dec-18 18759430 31-Dec-18 18742312 30-Nov-18 18730158 30-Nov-18 18700332 30-Nov-18 18666315 31-Oct-18 18642494 31-Oct-18 18598589 30-Sep-18 18598705 30-Sep-18 18590702 30-Sep-18 18571949 31-Aug-18 18576695 30-Sep-18 18542073 31-Aug-18 18553555 31-Aug-18 18461134 30-Jun-18 18487818 31-Jul-18 18482418 31-Jul-18 18455339 30-Jun-18 18790369 31-Jan-19 18790079 31-Jan-19 18759314 31-Dec-18 18700274 30-Nov-18 18700158 30-Nov-18 18676997 30-Nov-18 18676591 30-Nov-18 18642436 31-Oct-18 18620147 30-Sep-18 18633863 31-Oct-18 18473146 30-Jun-18 18482417 31-Jul-18 18473260 30-Jun-18 18433320 30-Jun-18 18419555 31-May-18 18406749 31-May-18 18398515 31-May-18 18811376 31-Jan-19 18825968 31-Jan-19 18816588 31-Jan-19 18790427 31-Jan-19 18790253 31-Jan-19 18700448 30-Nov-18 18629577 31-Oct-18 18660541 31-Oct-18 18642610 31-Oct-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-2163-2016%22
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