FDA Device recall Z-2174-2016
Target Detachable Coils: TARGET 360 NANO 2.5 MM X 4CM MODEL Number:M0035442540 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 2.5 MM X 4CM MODEL Number:M0035442540 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-2174-2016 |
| 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 2.5 MM X 4CM MODEL Number:M0035442540 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: M0035442540: Lot Number/Expiration Date: 18820098 31-Jan-19 18819974 31-Jan-19 18809411 31-Jan-19…MODEL Number: M0035442540: Lot Number/Expiration Date: 18820098 31-Jan-19 18819974 31-Jan-19 18809411 31-Jan-19 18809117 31-Jan-19 18768594 31-Dec-18 18736394 30-Nov-18 18654342 31-Oct-18 18554516 31-Aug-18 18489245 31-Jul-18 18416403 31-May-18 18393530 30-Apr-18 18820005 31-Jan-19 18778602 31-Dec-18 18735178 30-Nov-18 18760121 31-Dec-18 18583787 30-Sep-18 18583880 30-Sep-18 18778397 31-Dec-18 18778807 31-Dec-18 18760123 31-Dec-18 18469927 31-Jul-18 18455711 30-Jun-18 18441368 30-Jun-18 18820036 31-Jan-19 18809705 31-Jan-19 18760120 31-Dec-18 18654156 31-Oct-18 18606693 30-Sep-18 18521064 31-Jul-18 18808823 31-Jan-19 18808529 31-Jan-19 18787828 31-Jan-19 18758428 31-Dec-18 18654187 31-Oct-18 18654280 31-Oct-18 18583942 30-Sep-18 18521126 31-Jul-18 18469957 31-Jul-18 18831210 31-Jan-19 18758018 31-Dec-18 18654125 31-Oct-18 18521095 31-Jul-18 18462388 30-Jun-18 18456041 30-Jun-18 18455861 30-Jun-18 18830181 31-Jan-19 18820067 31-Jan-19 1 |
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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-2174-2016%22
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