FDA Device recall Z-2170-2016
Target Detachable Coils: TARGET HELICAL NANO 1.5 MM X 3 CM MODEL Number:M0035431530 Neurology: Target Detachable Coils are intended to endo…
- 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 HELICAL NANO 1.5 MM X 3 CM MODEL Number:M0035431530 Neurology: Target Detachable Coils are intended to endo… 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-2170-2016 |
| 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 HELICAL NANO 1.5 MM X 3 CM MODEL Number:M0035431530 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: M0035431530: Lot Number/Expiration Date: 18758254 31-Dec-18 18685258 30-Nov-18 18651285 31-Oct-18…MODEL Number: M0035431530: Lot Number/Expiration Date: 18758254 31-Dec-18 18685258 30-Nov-18 18651285 31-Oct-18 18637564 31-Oct-18 18426876 31-May-18 18802748 31-Jan-19 18758459 31-Dec-18 18709486 30-Nov-18 18637506 31-Oct-18 18551662 31-Aug-18 18551894 31-Aug-18 18551778 31-Aug-18 18503529 31-Jul-18 18466471 30-Jun-18 18841964 31-Jan-19 18829601 31-Jan-19 18758049 31-Dec-18 18767569 31-Dec-18 18685548 30-Nov-18 18651227 31-Oct-18 18551604 31-Aug-18 18830630 31-Jan-19 18843698 28-Feb-19 18842831 31-Jan-19 18637390 31-Oct-18 18592500 30-Sep-18 18557240 31-Aug-18 18627281 31-Oct-18 18776363 31-Dec-18 18767070 31-Dec-18 18732530 30-Nov-18 18551836 31-Aug-18 18453506 30-Jun-18 18815140 31-Jan-19 18814270 31-Jan-19 18780961 31-Jan-19 18766571 31-Dec-18 18637448 31-Oct-18 18522949 31-Jul-18 18518477 31-Jul-18 18801433 31-Jan-19 18777411 31-Dec-18 18735646 31-Dec-18 18734430 30-Nov-18 18685838 31-Oct-18 18722263 30-Nov-18 18458818 30-Jun-18 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-2170-2016%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.