# FDA recall Z-0265-2023

> **Medical Action Industries, Inc. 306** · Class II · device recall initiated 2022-09-15.

## 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.

## Distribution

US Nationwide distribution in the state of Pennsylvania.

## Key facts

- **Recall number:** Z-0265-2023
- **Recalling firm:** Medical Action Industries, Inc. 306
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-09-15
- **Report date:** 2022-11-30
- **Termination date:** 2025-02-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arden, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0265-2023

## Citation

> AI Analytics. FDA recall Z-0265-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0265-2023. Source: US FDA. Licensed CC0.

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