# FDA recall D-0049-2024

> **KVK-Tech, Inc.** · Class I · drug recall initiated 2023-09-20.

## Product

Betaxolol Tablets, USP 10 mg, Rx Only, 100 count bottles, Mfd by: KVK Tech Inc., Newtown, PA 18940, Made in USA, NDC# 10702-013-01.

## Reason for recall

Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles.

## Distribution

Nationwide in the USA and PR

## Key facts

- **Recall number:** D-0049-2024
- **Recalling firm:** KVK-Tech, Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2023-09-20
- **Report date:** 2023-10-25
- **Termination date:** 2025-07-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Newtown, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0049-2024

## Citation

> AI Analytics. FDA recall D-0049-2024. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/D-0049-2024. Source: US FDA. Licensed CC0.

---

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