FDA Device recall Z-2177-2016
Target Detachable Coils: TARGET 360 NANO 3.5 MM X 6CM MODEL Number:M0035443560 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 3.5 MM X 6CM MODEL Number:M0035443560 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-2177-2016 |
| 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 3.5 MM X 6CM MODEL Number:M0035443560 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:M0035443560: Lot Number/Expiration Date: 18736425 31-Dec-18 18521457 31-Jul-18 18838703 31-Jan-19 1…MODEL Number:M0035443560: Lot Number/Expiration Date: 18736425 31-Dec-18 18521457 31-Jul-18 18838703 31-Jan-19 18703233 30-Nov-18 18443288 30-Jun-18 18735209 30-Nov-18 18659056 31-Oct-18 18781251 31-Jan-19 18801665 31-Jan-19 18747459 31-Dec-18 18802980 31-Jan-19 18659087 31-Oct-18 18649087 31-Oct-18 18536525 31-Aug-18 19046694 31-May-19 19047725 31-May-19 18875709 28-Feb-19 18987089 30-Apr-19 19006438 30-Apr-19 18959391 31-Mar-19 18936943 31-Mar-19 19022830 30-Apr-19 18984771 30-Apr-19 18922696 31-Mar-19 18898321 28-Feb-19 19061363 31-May-19 18853805 28-Feb-19. |
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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-2177-2016%22
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