SUN PHARMACEUTICAL INDUSTRIES INC recalls Testosterone Cypionate Injection, USP, 200mg/ml, Rx Only, One Single-dose vial, Distributed by: Sun Pharmaceutical
Sun Pharmaceutical recalls specific lots of Testosterone Cypionate Injection due to manufacturing deviations causing abnormal machine parts. Affected lots have expiration dates through November 2022.
Recall notice
CGMP Deviations: Manufacturing deviations were reported due to an abnormal appearance on parts of machinery.
Contact the company & request your remedy
What happened, in plain English
Sun Pharmaceutical is recalling certain lots of Testosterone Cypionate Injection because of manufacturing issues that could affect product safety. This recall affects patients using the medication as prescribed by a doctor. Read more at govinfonow.com/recall/34659-sun-pharmaceutical-testosterone-cypionate-injection-recall-manufacturing-deviations.
Source Summary by GovInfoNow · govinfonow.com/recall/34659-sun-pharmaceutical-testosterone-cypionate-injection-recall-manufacturing-deviations · Updated September 23, 2026 · FDA enforcement record: FDA #D-1176-2022
Cite this page
“Sun Pharmaceutical Testosterone Cypionate Injection Recall: Manufacturing Deviations.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/34659-sun-pharmaceutical-testosterone-cypionate-injection-recall-manufacturing-deviations. Based on FDA recall #D-1176-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1176-2022%22&limit=1).
Why it’s dangerous
The recall is due to manufacturing deviations that caused abnormal appearance on parts of machinery. This could potentially lead to product quality issues, but the specific risk to patients is not clearly described in the recall notice.
Who’s affected
Patients prescribed Testosterone Cypionate Injection by a doctor who received the recalled lots. Those using the medication without a prescription are not affected.
How to tell if you have this one
Check the product label for the lot numbers JKX3267A, JKX3686A, JKX4700A, or JKX5727A with expiration dates through November 2022. The product is a single-dose vial of Testosterone Cypionate Injection, 200mg/ml, prescription-only.
- Brand
Sun Pharmaceutical- Category
Drug
What to do — step by step
Check Product Label
Look for lot numbers JKX3267A, JKX3686A, JKX4700A, or JKX5727A with expiration dates through November 2022.
Questions people ask
What is the recall about?
Sun Pharmaceutical is recalling specific lots of Testosterone Cypionate Injection due to manufacturing deviations that caused abnormal appearance on parts of machinery.
How can I tell if I have the recalled product?
Check the product label for lot numbers JKX3267A, JKX3686A, JKX4700A, or JKX5727A with expiration dates through November 2022.
What should I do if I have the recalled product?
The recall notice does not specify a remedy or action for affected products.
Contact Sun Pharmaceutical
We’ve drafted a message you can send Sun Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-1176-2022 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-1176-2022 from Sun Pharmaceutical. 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-1176-2022 (June 3, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1176-2022 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 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.