# FDA recall D-0216-2017

> **Sperian Eye & Face Protection, Inc** · Class I · drug recall initiated 2016-08-16.

## Product

Honeywell eyesaline Eyewash Sterile Isotonic Solution, sterile water 99%, 32 fl. oz. (946 ml.), Sperian Eye & Face Protection, Inc. (a Honeywell Company), Platteville, WI  53818

## Reason for recall

Non Sterility; contaminated with Klebsiella pneumoniae

## Distribution

Nationwide.  Outside the US to include:  Australia, Mexico and United Arab Emirates.

## Key facts

- **Recall number:** D-0216-2017
- **Recalling firm:** Sperian Eye & Face Protection, Inc
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-08-16
- **Report date:** 2016-12-28
- **Termination date:** 2019-05-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Platteville, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0216-2017

## Citation

> AI Analytics. FDA recall D-0216-2017. Retrieved 2026-07-01 from https://api.ai-analytics.org/recall/D-0216-2017. Source: US FDA. Licensed CC0.

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