FDA Recall Open, Classified

HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK, List Number MX497HP

Recall: Z-0744-2024 · Initiated November 10, 2023

Recall

Recall Number
Z-0744-2024
Event Number
93506
Firm
Smiths Medical Asd Inc
FEI Number
1526863
Product Code
DRS
Status
Open, Classified
Root Cause
Nonconforming Material/Component
Initiated
November 10, 2023
Posted
January 17, 2024
Address
6250 Shier Rings Rd, Dublin, OH, 43016-1270

Description

HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK, List Number MX497HP

Reason

There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication which may potentially lead to under infusion of medication.

Action

An URGENT MEDICAL DEVICE RECALL notification letter dated 11/10/23 was sent to customers. Required Actions for Users: 1. Please discontinue the use and distribution of the affected product immediately. Check your inventory and quarantine all affected product at your facility. 2. Inform potential users of the product in your organization of this notification and complete and return the attached response form to [email protected] within ten days of receipt to acknowledge your understanding of this notification, even if you do not have the affected product and/or it has already been used. 3. If you have distributed the product further, immediately notify your accounts that receive the product identified in the Affected Items / Table 1 sections of this notification and ask them to contact Sedgwick at 1-855-215-5142 (MF, 8am-5pm ET) to obtain a response form. 4. If the product has not already been used, please return affected lots to Smiths Medical and Smiths Medical will offer replacement units. Global Complaint Management [email protected] 1-(866)-216-8806 Customer Service 1-(800)-258-5361

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, UAE.

Quantity

31,685 total