# FDA recall Z-1531-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2025-02-19.

## Product

Wayson Hydrocolloid Models:  1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT, Model Number: MJ18004V2;   2) MJ BANDAGE HYDROCOLLOID ALL PURP 10CT, Model Number: MJ18005V2;   3) MJ BNDG HYDROCOLLOID FINGER TOE 8CT, Model Number: MJ76126V2;   4) WALMART,BANDAGE,HYDROCOLLOID,HEEL,6CT, Model Number: WAL1901;   5) WALMART,HYDROCOLLOID,TOE,8CT, Model Number: WAL1902;

## Reason for recall

There is a potential for the sterility of the device to be compromised.

## Distribution

Worldwide Distribution: US (Nationwide) and OUS (Foreign) to countries of: Bermuda, Canada, Panama, Singapore

## Key facts

- **Recall number:** Z-1531-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-19
- **Report date:** 2025-04-16

- **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-1531-2025

## Citation

> AI Analytics. FDA recall Z-1531-2025. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1531-2025. Source: US FDA. Licensed CC0.

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