# FDA recall D-0167-2020

> **Arbor Pharmaceuticals Inc.** · Class III · drug recall initiated 2019-09-27.

## Product

Testosterone Cypionate Injection, USP, 2000 mg/10 mL, 1 mL Vial, Single-Dose,  Rx only, Mfd. for: Wilshire Pharmaceuticals, Inc. Atlanta, GA 30328. NDC 52536-625-01

## Reason for recall

Labeling:Label Mix-up: Shipper Carton labelled Testosterone Cypionate Injection, USP, 200mg/mL, 1 ml single-dose  vials, found to contain shelf cartons labelled as Testosterone Cypionate Injection USP, 200mg/mL, 10 ml  multi-dose vials which contain Testosterone Cypionate Injection USP, 200mg/mL,1mL single-does vials

## Distribution

Nationwide in the US

## Key facts

- **Recall number:** D-0167-2020
- **Recalling firm:** Arbor Pharmaceuticals Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-09-27
- **Report date:** 2019-11-06
- **Termination date:** 2021-02-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Atlanta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0167-2020

## Citation

> AI Analytics. FDA recall D-0167-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0167-2020. Source: US FDA. Licensed CC0.

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