FDA Recall Open, Classified

Prelude IDEAL 4 F Hydrophilic Sheath Introducer, REF: PID4F16021PW/D

Recall: Z-1434-2025 · Initiated January 27, 2025

Recall

Recall Number
Z-1434-2025
Event Number
96292
Firm
Merit Medical Systems, Inc.
FEI Number
1721504
Product Code
DYB
Status
Open, Classified
Root Cause
Packaging process control
Initiated
January 27, 2025
Posted
March 24, 2025
Address
1600 W Merit Pkwy South, Jordan, UT, 84095-2416

Description

Prelude IDEAL 4 F Hydrophilic Sheath Introducer, REF: PID4F16021PW/D

Reason

Hydrophilic Sheath Introducer labeled for 4F dilators may instead incorrectly contain 5F dilators. Incorrect dilator use may result in procedure delay.

Action

On 1/27/2025, recall notices were sent to customers asking them to do the following: 1) Quarantine, and discontinue use and distribution of affected devices. 2) Return all affected lots in your possession to the recalling firm. 3) Ensure that applicable personnel within your organization are made aware of this field action. 4) If the product has been further distributed to other facilities, institutions, or manufacturers, please ensure this notice is immediately shared with them and note the quantity distributed on the CRF. Questions can be directed to Customer Service via email at [email protected] or via phone at +1 800 356 3748, Hours: 6 am to 6 pm MST, Mon-Fri.

Distribution

International distribution to the country of Japan.

Quantity

40