# FDA recall Z-3054-2020

> **Medline Industries Inc** · Class II · device recall initiated 2020-07-28.

## Product

Control, Calibrator Verified, Triage BNP, Model ALR88755

## Reason for recall

Product was shipped with refrigeration (ice) instead of frozen (dry ice).

## Distribution

Distribution in US - AR, AZ, CO, FL, MD, MS, MI, NC, NM, NY, OK, PA, RI, TX

## Key facts

- **Recall number:** Z-3054-2020
- **Recalling firm:** Medline Industries Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-07-28
- **Report date:** 2020-10-07
- **Termination date:** 2023-02-13

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3054-2020

## Citation

> AI Analytics. FDA recall Z-3054-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-3054-2020. Source: US FDA. Licensed CC0.

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