FDA Recall Open, Classified

Prelude Sheath Introducer 7.5F, REF: PSI-7F-11-038 Version F (PSI-7F-11-038/F)

Recall: Z-3190-2024 · Initiated August 12, 2024

Recall

Recall Number
Z-3190-2024
Event Number
95234
Firm
Merit Medical Systems, Inc.
FEI Number
1721504
Product Code
DRE
Status
Open, Classified
Root Cause
Labeling mix-ups
Initiated
August 12, 2024
Posted
September 20, 2024
Address
1600 W Merit Pkwy South, Jordan, UT, 84095-2416

Description

Prelude Sheath Introducer 7.5F, REF: PSI-7F-11-038 Version F (PSI-7F-11-038/F)

Reason

7F sheath introducers labeled as 7.5F

Action

On 8/12/24, recall notices were mailed or emailed to customers who were asked to do the following: 1) Determine if any of the products identified in the attached Customer Response From (CRF) are within your facility. 2) Ensure that appropriate personnel within your organization are made aware of this field action. 3) If the product has been further distributed to other facilities, institutions, or manufacturers, ensure this notice is immediately shared with them. Additional distribution details may be required by health authorities. 4) Post this "URGENT MEDICAL DEVICE RECALL NOTICE" on or near the affected products. Product may continue to be used once this recall notice is placed on or near them. 5) Complete and return the response form via email to [email protected] If you have any questions concerning this communication, contact the firm's Sales Representative or Customer Service at +1 800 356 3748 | Hours: 6 am to 6 pm MST, Mon-Fri.

Distribution

Worldwide - US Nationwide distribution in the states of WI, MN, TX, PA, GA, NE, CA, AR, MS, MA, MI, OH, CO, NV, OR, AZ, NC and the country of Mexico.

Quantity

1892