# FDA recall Z-0806-2018

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2018-02-06.

## Product

Sterile EXACTAMED Oral Dispenser, Clear, Individually Packaged, 5 mL, Product Code H93876105

## Reason for recall

Affected lot of 5 mL oral dispensers was packaged in individual pouches that are mislabeled with the incorrect product code (H93876101) and volume (1mL).

## Distribution

Distributed domestically to IL, MA, MD, OH, SD, TX, VA, WI.      Distributed internationally to Canada.

## Key facts

- **Recall number:** Z-0806-2018
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-02-06
- **Report date:** 2018-03-07
- **Termination date:** 2021-04-02

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0806-2018

## Citation

> AI Analytics. FDA recall Z-0806-2018. Retrieved 2026-05-23 from https://api.ai-analytics.org/recall/Z-0806-2018. Source: US FDA. Licensed CC0.

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