B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)
FDA Recall Z-0265-2023 · Posted 2022-11-18
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Recalling FirmMedical Action Industries, Inc. 306
Recall StatusTerminated
Product CodeOFF
Date Initiated2022-09-15
Date Terminated2025-02-19
Product Quantity240 cases of 20 units
Reason for Recall
The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024.
Firm Action
Owens & Minor/Medical Action INDUSTRIES, INC. issued an URGENT: MEDICAL DEVICE FIELD CORRECTION to its sole consignee on 09/23/2022 by email. The notices explained the issue and requested they take the following actions: "Please review your inventory, and segregate and quarantine all affected Kits. If any of the affected kits identified above were further distributed, please ensure all end-users are appropriately notified and maintain records of effectiveness.
A labeling template is enclosed for printing labels which can be affixed on all affected kits in inventory. This label should be applied to each affected convenience kit and product case in a prominently visible location to end-users. The location chosen should not cover any other critical product information found on existing product labeling. If you prefer to have labels printed for your facility, please send quantity and end-user information to [email protected].
Any adverse events associated with the use of the affected products should be reported to [email protected].
The FDA requires that we account for all affected products. Therefore, please complete the attached Response Form and return to [email protected] as soon as possible even if you have no current product inventory.
If you have any questions, please send an email to [email protected]."
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution in the state of Pennsylvania.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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