# FDA recall D-0421-2018

> **Webrx dba RxPalace.com** · Class III · drug recall initiated 2018-02-07.

## Product

BonaDur For Men (lidocaine) spray, 10 mg per spray, Net Contents .25 fl. oz. (7.4 mL) spray bottles, Manufactured by WebRx Pharmacy Palace, Sarasota, FL 34232; NDC 70582-999-74

## Reason for recall

CGMP Deviations: not manufactured according to current good manufacturing practices.

## Distribution

NY

## Key facts

- **Recall number:** D-0421-2018
- **Recalling firm:** Webrx dba RxPalace.com
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-02-07
- **Report date:** 2018-02-21
- **Termination date:** 2020-05-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sarasota, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0421-2018

## Citation

> AI Analytics. FDA recall D-0421-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0421-2018. Source: US FDA. Licensed CC0.

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