# FDA recall D-0695-2017

> **Fagron, Inc** · Class III · drug recall initiated 2017-04-17.

## Product

Zinc Oxide Paste 25%, 500 g, For Prescription Compounding, Fagron Inc.2400 Pilot Knob Rd, St. Paul, MN 55120m  NDC 51522-0694-5.

## Reason for recall

Labeling: Error on Declared Strength: Error is due to an incorrect value in the Drug Facts Panel. The correct strength is displayed on the primary container.

## Distribution

Nationwide within US

## Key facts

- **Recall number:** D-0695-2017
- **Recalling firm:** Fagron, Inc
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-04-17
- **Report date:** 2017-05-10
- **Termination date:** 2017-08-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Paul, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0695-2017

## Citation

> AI Analytics. FDA recall D-0695-2017. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0695-2017. Source: US FDA. Licensed CC0.

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