B — Class II medical device recall Z-0265-2023
Terminated recall by Medical Action Industries, Inc. 306, reported 2022-11-30, distributed nationwide. The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024.
| Recall number | Z-0265-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Action Industries, Inc. 306, Arden, NC, United States |
| Recall initiated | 2022-09-15 |
| Classified | 2022-11-18 |
| Reported by FDA | 2022-11-30 |
| Terminated | 2025-02-19 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 10809160283875 |
| Lot numbers | 298442 |
| Model numbers | 375214 |
Product
B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)
Reason for recall
The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0265-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.