# FDA recall D-0482-2019

> **US Compounding Inc** · Class II · drug recall initiated 2019-01-24.

## Product

LET Gel 4% (Lidocaine HCl 4% + EPINEPHrine HCl 0.05% + Tetracaine HCl 0.5%), 3mL Single Use Syringe, Rx only, US Compounding, 1270 Don's Lane, Conway, AR, 800-718-3588, Barcode 62295501303.

## Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp Date: Labels are missing lot and expiration date and are printed as Lot# YYYDDYY@XX with a Beyond Use Date: MM/DD/YYY.

## Distribution

Nationwide in the USA.

## Key facts

- **Recall number:** D-0482-2019
- **Recalling firm:** US Compounding Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-01-24
- **Report date:** 2019-02-20
- **Termination date:** 2020-01-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Conway, AR, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0482-2019

## Citation

> AI Analytics. FDA recall D-0482-2019. Retrieved 2026-06-01 from https://api.ai-analytics.org/recall/D-0482-2019. Source: US FDA. Licensed CC0.

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