Prelude IDEAL 4 F Hydrophilic Sheath Introducer, REF: PID4F16021PW/D
FDA Recall Z-1434-2025 · Posted 2025-03-24
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Recalling FirmMerit Medical Systems, Inc.
Recall StatusOpen, Classified
Product CodeDYB
Date Initiated2025-01-27
Product Quantity40
Reason for Recall
Hydrophilic Sheath Introducer labeled for 4F dilators may instead incorrectly contain 5F dilators. Incorrect dilator use may result in procedure delay.
Firm 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.
Root Cause
Packaging process control
Distribution Pattern
International distribution to the country of Japan.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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