Testosterone Cypionate Injection — Class III drug recall D-0167-2020
Terminated recall by Arbor Pharmaceuticals Inc., reported 2019-11-06, distributed nationwide. Labeling:Label Mix-up: Shipper Carton labelled Testosterone Cypionate Injection, USP, 200mg/mL, 1 ml single-do
| Recall number | D-0167-2020 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arbor Pharmaceuticals Inc., Atlanta, GA, United States |
| Recall initiated | 2019-09-27 |
| Classified | 2019-10-30 |
| Reported by FDA | 2019-11-06 |
| Terminated | 2021-02-02 |
| Distributed | Nationwide (US) |
| Quantity | 67,934 units |
| Reason classes | labeling |
| NDC | 52536-0625, 52536-0625-01, 52536-0625-10 |
| Lot numbers | 23803.002B, 23803.005A |
| Expiration dates | 2020-07, 2021-01 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0167-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.