FDA Device recall Z-0265-2023
B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)
- FDA Device
- Class II
- terminated
- Published 2022-11-30
On 2022-11-30 the FDA classified a Class II recall of B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022) by Medical Action Industries 306, citing the kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0265-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-09-15 |
| Published | 2022-11-30 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medical Action Industries 306 |
| Distribution | US |
Product
B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)
Reason
The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024.
Identifiers
| code_info | UDI/DI 10809160283875, Batch/Lot number 298442 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0265-2023%22
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