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Recall Observatory FDA recall evidence

Device product

6F/7F MynxGrip Vascular Closure Device; Product Model MX6721, Product Usage: The 6F/7F MynxGrip Vascular Closure Device is indicated for use to seal femoral arterial and femoral venous access sites while reducing times to hemostasis and ambulation in patients who have undergone diagnostic or interventional endovascular procedures utilizing a 6F or 7F procedural sheath. The 6F/7F MynxGrip Vascular Closure Device is designed to achieve femoral artery and femoral vein hemostasis via delivery of an extravascular, water-soluble synthetic sealant using a balloon catheter in conjunction with a standard procedural sheath. The sealant is comprised of a polyethylene glycol (PEG) material which expands upon contact with subcutaneous fluids to seal the arteriotomy or venotomy. The sealant is resorbed by the body within 30-days.

Z-2329-2016

July 13, 2016

Class II

Product summary

Firm
AccessClosure, Inc., A Cardinal Health Company
Event
Event 74599
Status
Terminated
Classification
Class II
Quantity
55 units
Official record key
device-enforcement:Z-2329-2016

Official wording

Reason: A total of 70 6F/7F Mynx Grip devices were shipped from a distributor using improper transport/packaging configurations.

Code information: Lot No: F1609702, Expiry 4/20/2018; Lot No. F1534302, Expiry 12/31/2016

Distribution pattern: US in the states of CA, and MS.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    A total of 70 6F/7F Mynx Grip devices were shipped from a distributor using improper transport/packaging configurations.