# FDA recall D-0648-2022

> **Revive Rx LLC dba Revive Rx Pharmacy** · Class I · drug recall initiated 2022-02-11.

## Product

HCG 6,000iu (lyo) Human Chorionic Gonadotropin Inj., For Sub-Q or IM Use Only, Not For IV Use, Vial, Rx Only, Compounded By: Revive Rx 3831 Golf Dr., Houston, TX 77018, NDC: 88888-1739-01.

## Reason for recall

Non-sterility; bacterial contamination identified as Paenibacillus lautus.

## Distribution

Nationwide in the US.

## Key facts

- **Recall number:** D-0648-2022
- **Recalling firm:** Revive Rx LLC dba Revive Rx Pharmacy
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-02-11
- **Report date:** 2022-02-23
- **Termination date:** 2024-08-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Houston, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0648-2022

## Citation

> AI Analytics. FDA recall D-0648-2022. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/D-0648-2022. Source: US FDA. Licensed CC0.

---

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