# FDA recall D-0250-2019

> **Kadesh International** · Class I · drug recall initiated 2018-11-05.

## Product

puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0.

## Reason for recall

Non-Sterility: Product manufactured under non-sterile production conditions.

## Distribution

Product was distributed via online stores and retail distributors Nationwide in the USA, Uruguay, Canada, China, Dominican Republic, Korea, and Vietnam.

## Key facts

- **Recall number:** D-0250-2019
- **Recalling firm:** Kadesh International
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-11-05
- **Report date:** 2018-11-21
- **Termination date:** 2023-01-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Garden Grove, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0250-2019

## Citation

> MORVS. FDA recall D-0250-2019. Retrieved 2026-10-21 from https://api.morvs.ai/recall/D-0250-2019. Source: US FDA. Licensed CC0.

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