Cordis US Corp: Medical Device Recall in 2024 - (Recall #: Z-0675-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

MYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites

Product Classification:

Class II

Date Initiated: November 28, 2023

Date Posted: January 17, 2024

Recall Number: Z-0675-2024

Event ID: 93617

Reason for Recall:

Cordis became aware that the label for the carton box containing 10 units is incorrect for some boxes of two lots of MynxGrip. The carton box from lot F2322902 (Item MX5021, MynxGrip 5F) as labeled as lot F2322903 (MX6721, MynxGrip 6/7F) and product from lot F2322903 (MX6721, MynxGrip 6/7F) was labeled as F2322902 (Item MX5021, MynxGrip 5F). The primary label on individual devices is correct.

Status: Ongoing

Product Quantity: 70 units

Code Information:

UDI/DI 10862028000403, Lot numbers: F2322903

Distribution Pattern:

US: NC, WV, TN, MS, MI, OH, CA

Voluntary or Mandated:

Voluntary: Firm initiated