# FDA recall Z-0088-2019

> **MEDLINE INDUSTRIES INC** · Class II · device recall initiated 2018-08-30.

## Product

Unna-Z: Unna Boot Compression Wrap with Zinc Oxide and Calamine, Item Numbers:  a) NONUNNA3 and b) NONUNNA4    Product is packaged in a foil pouch, which is inserted in a box carton.  There are 12 cartons in each case.

## Reason for recall

Firm received sporadic reports of discoloration on certain lots of the product, which has been identified as common mold.

## Distribution

United States, Taiwan, Chile

## Key facts

- **Recall number:** Z-0088-2019
- **Recalling firm:** MEDLINE INDUSTRIES INC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-08-30
- **Report date:** 2018-10-17
- **Termination date:** 2023-02-09

- **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-0088-2019

## Citation

> AI Analytics. FDA recall Z-0088-2019. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-0088-2019. Source: US FDA. Licensed CC0.

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