RecallRadar

FDA Device recall Z-2180-2016

Target Detachable Coils: TARGET HELICAL NANO 2MM X 4CM MODEL Number:M0035452040 Neurology: Target Detachable Coils are intended to endovasc…

On 2016-07-20 the FDA classified a Class II recall of Target Detachable Coils: TARGET HELICAL NANO 2MM X 4CM MODEL Number:M0035452040 Neurology: Target Detachable Coils are intended to endovasc… 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

AgencyFDA Device
Recall numberZ-2180-2016
ClassificationClass II
Statusterminated
Initiated2016-06-06
Published2016-07-20
Last updated2026-09-13 11:54 UTC
CompanyStryker Neurovascular
DistributionUS

Product

Target Detachable Coils: TARGET HELICAL NANO 2MM X 4CM MODEL Number:M0035452040 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:M0035452040; Lot Number/Expiration Date: 18760131 31-Dec-18 18760129 31-Dec-18 18832208 31-Jan-19 1…MODEL Number:M0035452040; Lot Number/Expiration Date: 18760131 31-Dec-18 18760129 31-Dec-18 18832208 31-Jan-19 18832819 31-Jan-19 18831597 31-Jan-19 18760132 31-Dec-18 18760130 31-Dec-18 18852438 28-Feb-19 18905625 31-Mar-19 18939389 31-Mar-19 19032961 30-Apr-19 19032868 30-Apr-19 19037908 31-May-19 18900809 28-Feb-19 18906580 28-Feb-19 18987592 30-Apr-19 19036655 31-May-19 18971469 30-Apr-19 18986652 30-Apr-19 18875322 28-Feb-19 19047456 31-May-19 18972020 30-Apr-19 18899967 28-Feb-19.

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-2180-2016%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.