# FDA recall Z-1256-2021

> **Cardinal Health 200, LLC** · Class II · device recall initiated 2021-02-11.

## Product

JUDKINS PACK

## Reason for recall

Component Part Number: 19537LBL (LBL, SHEET OF 39, ASSORTED, STDSZ, MULTI W/BLK INK, WATERPROOF) is being reported as intermittently mixed with an incorrect medication label sheet throughout the specific Presource¿ kit SANHDJTVCF Judkins Pack lot # 525067.

## Distribution

US state of VA.

## Key facts

- **Recall number:** Z-1256-2021
- **Recalling firm:** Cardinal Health 200, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-02-11
- **Report date:** 2021-03-24
- **Termination date:** 2022-12-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukegan, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1256-2021

## Citation

> AI Analytics. FDA recall Z-1256-2021. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1256-2021. Source: US FDA. Licensed CC0.

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