Medex 700PSI STOPCOCK W/ROTATOR, List Number MX4331R
FDA Recall Z-0742-2024 · Posted 2024-01-17
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Recalling FirmSmiths Medical Asd Inc
Recall StatusOpen, Classified
Product CodeDRS
Date Initiated2023-11-10
Product Quantity31,685 total
Reason for Recall
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.
Firm 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
Root Cause
Nonconforming Material/Component
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of Canada, UAE.
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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