# FDA recall Z-1752-2022

> **CAREFUSION** · Class II · device recall initiated 2022-08-01.

## Product

BD MaxGuard Extension Set with 4-way stopcock, REF: M4058

## Reason for recall

Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

## Distribution

US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN

## Key facts

- **Recall number:** Z-1752-2022
- **Recalling firm:** CAREFUSION
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-08-01
- **Report date:** 2022-09-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Diego, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1752-2022

## Citation

> AI Analytics. FDA recall Z-1752-2022. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-1752-2022. Source: US FDA. Licensed CC0.

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