# FDA recall Z-1059-2023

> **Owens & Minor Distribution, Inc.** · Class III · device recall initiated 2023-01-03.

## Product

FLUIDSHIELD 3 Fog-Free Procedure Mask with SO SOFT Lining and SO SOFT Earloops, Orange, WrapAround Visor    Product Code 47147

## Reason for recall

Face masks were placed into the incorrect dispenser boxes. The face masks come with ear loops, but the dispenser is incorrectly labeled as face masks with ties instead of ear loops.

## Distribution

US distribution to IL, NC, NY, OH, and PA.

## Key facts

- **Recall number:** Z-1059-2023
- **Recalling firm:** Owens & Minor Distribution, Inc.
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-01-03
- **Report date:** 2023-02-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mechanicsville, VA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1059-2023

## Citation

> AI Analytics. FDA recall Z-1059-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1059-2023. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
