Arbor Pharmaceuticals Inc. recalls Testosterone Cypionate Injection, USP, 2000 mg/10 mL, 1 mL Vial, Single-Dose, Rx only, Mfd. for: Wilshire
Arbor Pharmaceuticals recalls Testosterone Cypionate Injection vials due to labeling mix-up. The product may contain incorrect strength and dosage. Consumers should check product details and contact the manufacturer for clarification.
Lower-risk 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
Contact the company & request your remedy
What happened, in plain English
Arbor Pharmaceuticals is recalling Testosterone Cypionate Injection vials because the labeling shows a mix-up in the product's strength and dosage. This could lead to incorrect dosing if used without proper verification. Read more at govinfonow.com/recall/37896-arbor-pharmaceuticals-testosterone-cypionate-injection-recall-label-mix-up-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/37896-arbor-pharmaceuticals-testosterone-cypionate-injection-recall-label-mix-up-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-0167-2020
Cite this page
“Arbor Pharmaceuticals Testosterone Cypionate Injection Recall: Label Mix-Up Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37896-arbor-pharmaceuticals-testosterone-cypionate-injection-recall-label-mix-up-risk. Based on FDA recall #D-0167-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0167-2020%22&limit=1).
Why it’s dangerous
The vials are labeled with incorrect strength information. The product may contain single-dose vials that are mistakenly labeled as multi-dose vials, leading to potential dosing errors if used without proper verification.
Who’s affected
Individuals who have purchased or received Testosterone Cypionate Injection vials from Arbor Pharmaceuticals. Those using the product for medical purposes are most at risk due to potential dosing errors.
How to tell if you have this one
Check for the NDC code 52536-625-01 or lot numbers 23803.002B (exp 07/2020) or 23803.005A (exp 01/2021). The product is sold under the brand name Testosterone Cypionate Injection, USP, 2000 mg/10 mL, 1 mL vial.
- Brand
Arbor Pharmaceuticals- Category
Drug
What to do — step by step
Check Product Details
Verify the NDC code and lot number on the vial to confirm it matches the recalled product.
Questions people ask
What is the specific product being recalled?
Testosterone Cypionate Injection, USP, 2000 mg/10 mL, 1 mL Vial, Single-Dose, Rx only, with NDC 52536-625-01 or lot numbers 23803.002B (exp 07/2020) or 23803.005A (exp 01/2021).
Why is this product being recalled?
The recall is due to a labeling mix-up where the product may contain incorrect strength and dosage information.
What should I do if I have this product?
Check the product details to confirm it matches the recalled product. Contact Arbor Pharmaceuticals for further guidance.
Contact Arbor Pharmaceuticals
We’ve drafted a message you can send Arbor Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0167-2020 — Arbor Pharmaceuticals Arbor Pharmaceuticals Hello, I own a Arbor Pharmaceuticals that is covered by recall D-0167-2020 from Arbor Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0167-2020 (September 27, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0167-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.