Stryker Neurovascular: Medical Device Recall in 2016 - (Recall #: Z-2179-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Target Detachable Coils: TARGET HELICAL NANO 2MM X 3CM MODEL Number:M0035452030 Neurology: Target Detachable Coils are intended to endovascularly obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels.

Product Classification:

Class II

Date Initiated: June 6, 2016

Date Posted: July 20, 2016

Recall Number: Z-2179-2016

Event ID: 74425

Reason for Recall:

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.

Status: Terminated

Product Quantity: 45,302 (8,188 in the U.S.) - total, all model numbers

Code Information:

MODEL Number::M0035452030; Lot Number/Expiration Date: 19032837 30-Apr-19 19034203 31-May-19 18953644 31-Mar-19 19032930 30-Apr-19 18986505 30-Apr-19 18922370 31-Mar-19 18987445 30-Apr-19 18972051 30-Apr-19 18971500 30-Apr-19 18905990 31-Mar-19 19060369 31-May-19.

Distribution Pattern:

Worldwide Distribution - US (nationwide) and Australia, Austria, Belgium, Brazil, Bulgaria, Canada, Canary Islands, Chile, China, Colombia, Croatia, Czech Republic, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Ireland, Italia, Japan,Latvia, Lebanon, Libyan Arab Jamahiriya, Lithuania, Luxembourg, Mexico,Netherlands, Norway, Peru, Philippines, Poland, Portugal, Russia, Saudi Arabia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, and Vietnam.

Voluntary or Mandated:

Voluntary: Firm initiated