FDA Device recall Z-2162-2016
Target Detachable Coils: TARGET 360 NANO 1.5 MM X 2 CM MODEL Number: M0035421520 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 2 CM MODEL Number: M0035421520 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-2162-2016 |
| 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 2 CM MODEL Number: M0035421520 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: M0035421520: Lot Number/Expiration Date: 18571775 31-Aug-18 18826432 31-Jan-19 18820709 31-Jan-19 18…MODEL Number: M0035421520: Lot Number/Expiration Date: 18571775 31-Aug-18 18826432 31-Jan-19 18820709 31-Jan-19 18810506 31-Jan-19 18771506 31-Dec-18 18742834 31-Dec-18 18641914 31-Oct-18 18660947 31-Oct-18 18432978 30-Jun-18 18825388 31-Jan-19 18810970 31-Jan-19 18820593 31-Jan-19 18758780 31-Dec-18 18789731 31-Jan-19 18742776 31-Dec-18 18721938 30-Nov-18 18676533 30-Nov-18 18633805 31-Oct-18 18641972 31-Oct-18 18825910 31-Jan-19 18826258 31-Jan-19 18701086 30-Nov-18 18742718 31-Dec-18 18676359 30-Nov-18 18700796 30-Nov-18 18666663 31-Oct-18 18625251 31-Oct-18 18642030 31-Oct-18 18598415 30-Sep-18 18534255 31-Aug-18 18821173 28-Feb-19 18810390 31-Jan-19 18789847 31-Jan-19 18789673 31-Jan-19 18758370 31-Dec-18 18728186 30-Nov-18 18700680 30-Nov-18 18625135 30-Sep-18 18576927 30-Sep-18 18534545 31-Aug-18 18487470 31-Jul-18 18460621 30-Jun-18 18826084 31-Jan-19 18825736 31-Jan-19 18825562 31-Jan-19 18810738 31-Jan-19 18820941 31-Jan-19 188 |
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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-2162-2016%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.