FDA Device recall Z-2173-2016
Target Detachable Coils: TARGET 360 NANO 2MM X 4CM MODEL Number:M0035442040 Neurology: Target Detachable Coils are intended to endovascular…
- 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 2MM X 4CM MODEL Number:M0035442040 Neurology: Target Detachable Coils are intended to endovascular… 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-2173-2016 |
| 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 2MM X 4CM MODEL Number:M0035442040 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: M0035442040: Lot Number/Expiration Date: 18824889 31-Jan-19 18789584 31-Jan-19 18715147 30-Nov-18…MODEL Number: M0035442040: Lot Number/Expiration Date: 18824889 31-Jan-19 18789584 31-Jan-19 18715147 30-Nov-18 18654621 31-Oct-18 18583663 31-Aug-18 18779217 31-Dec-18 18771773 31-Dec-18 18758989 31-Dec-18 18715561 30-Nov-18 18567945 31-Aug-18 18583694 30-Sep-18 18489927 31-Jul-18 18456251 30-Jun-18 18456101 30-Jun-18 18779279 31-Dec-18 18789344 31-Jan-19 18771711 31-Dec-18 18715383 30-Nov-18 18679151 30-Nov-18 18568131 31-Aug-18 18470407 30-Jun-18 18818239 31-Jan-19 18810301 31-Jan-19 18721156 30-Nov-18 18702459 30-Nov-18 18521395 31-Jul-18 18824769 31-Jan-19 18779248 31-Dec-18 18702490 30-Nov-18 18654590 31-Oct-18 18436562 30-Jun-18 18825009 31-Jan-19 18818208 31-Jan-19 18810061 31-Jan-19 18702552 30-Nov-18 18741929 30-Nov-18 18667537 31-Oct-18 18567883 31-Aug-18 18456191 30-Jun-18 18440768 30-Jun-18 18824649 31-Jan-19 18810181 31-Jan-19 18809941 31-Jan-19 18758869 31-Dec-18 18741991 30-Nov-18 18741898 30-Nov-18 18568007 31-Aug-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-2173-2016%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.