PlainRecalls
FDA Devices Moderate Class II Ongoing

COBRA-OS, custom Sheath Introducer Kit, 4 French, REF: E01P2, Sterile EO, Single Use, RX Only, 5 Units

Reported: May 17, 2023 Initiated: March 21, 2023 #Z-1578-2023

Product Description

COBRA-OS, custom Sheath Introducer Kit, 4 French, REF: E01P2, Sterile EO, Single Use, RX Only, 5 Units

Reason for Recall

Custom sheath Introducer contains incorrect needle size

Details

Units Affected
1186 units
Distribution
US Distribution to state of: Minnesota
Location
South Jordan, UT

Frequently Asked Questions

What product was recalled?
COBRA-OS, custom Sheath Introducer Kit, 4 French, REF: E01P2, Sterile EO, Single Use, RX Only, 5 Units. Recalled by Merit Medical Systems, Inc.. Units affected: 1186 units.
Why was this product recalled?
Custom sheath Introducer contains incorrect needle size
Which agency issued this recall?
This recall was issued by the FDA Devices on May 17, 2023. Severity: Moderate. Recall number: Z-1578-2023.