# FDA recall Z-0025-2024

> **Becton Dickinson Infusion Therapy Systems Inc.** · Class II · device recall initiated 2023-08-29.

## Product

REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA  1.00 IN,  1.1 x 25 mm 64 mL/min , Rx Only, Sterile EO

## Reason for recall

There is the potential that the safety shield may not properly engage on IV catheters. The needle can pull through the safety shield and disconnect from the needle safety shield leaving the contaminated needle point exposed.

## Distribution

US Nationwide distribution in the states of CA, FL, GA, MA, MN, MO, MS, NJ, OH, TX.

## Key facts

- **Recall number:** Z-0025-2024
- **Recalling firm:** Becton Dickinson Infusion Therapy Systems Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-29
- **Report date:** 2023-10-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sandy, UT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0025-2024

## Citation

> AI Analytics. FDA recall Z-0025-2024. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/Z-0025-2024. Source: US FDA. Licensed CC0.

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