Sun Pharmaceutical Industries, Inc. recalls Testosterone Cypionate for Injection, USP, 1,000 mg/10 mL (100 mg/mL), 10 mL Multiple Dose Vial (NDC 62756-017-40), Rx
Sun Pharmaceutical recalls specific testosterone injection vials due to manufacturing quality deviations. Affected lots were produced under similar conditions to a previously rejected batch. Consumers should contact the manufacturer for details.
Lower-risk recall
cGMP Deviations; released lots were manufactured under similar manufacturing conditions to a previously rejected OOS Lot.
Contact the company & request your remedy
What happened, in plain English
Sun Pharmaceutical is recalling certain testosterone injection vials because they were made under similar conditions to a previously rejected batch. This could lead to quality issues with the product. Read more at govinfonow.com/recall/37473-sun-pharmaceutical-testosterone-cypionate-injection-recall-manufacturing-quality-issues.
Source Summary by GovInfoNow · govinfonow.com/recall/37473-sun-pharmaceutical-testosterone-cypionate-injection-recall-manufacturing-quality-issues · Updated October 5, 2026 · FDA enforcement record: FDA #D-0787-2020
Cite this page
“Sun Pharmaceutical Testosterone Cypionate Injection Recall: Manufacturing Quality Issues.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37473-sun-pharmaceutical-testosterone-cypionate-injection-recall-manufacturing-quality-issues. Based on FDA recall #D-0787-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0787-2020%22&limit=1).
Why it’s dangerous
The recalled vials were manufactured under similar conditions to a previously rejected batch that had quality issues. This means the product may not meet the required standards for safe medical use.
Who’s affected
People who have received the recalled testosterone injections from Sun Pharmaceutical. Those using the product for medical purposes are most at risk.
How to tell if you have this one
Check the product label for the NDC code 62756-017-40. The affected vials have specific expiration dates listed in the recall notice.
- Brand
Sun Pharmaceutical- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Product was distributed throughout the United States.- NDC
62756-017-40, 62756-015-40, 62756-016-40
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0787-2020 | Testosterone Cypionate for Injection, USP, 1,000 mg/10 mL (100 mg/mL), 10 mL Multiple Dose Vial (NDC 62756-017-40), Rx only, Distributed by: Sun Pharmaceuticals, Inc., Cranbury, NJ, Manufactured by: Sun Pharmaceuticals, Industries, Ltd., Gujarat, India; JKT0933A, JKT0935A, JKT1062A exp Mar-20; JKT1425A, JKT1483A exp Apr-20; JKT1575A, JKT1729A, JKT1730A, JKT1728A exp May-20 JKT2002A exp Jun-20; JKT3216A, JKT3217A exp Sep-20; JKT3589A, JKT3590A, JKT3626A exp Oct-20; JKT3864A, JKT3935A exp Dec-20 | — |
| D-0788-2020 | Testosterone Cypionate for Injection, 2,000 mg/10 mL (200 mg/mL), a) 1 mL Single Use vial (NDC 62756-015-40) and b) 10 mL Multiple Dose Vial (NDC 62756-016-40), Rx only, Distributed by: Sun Pharmaceuticals, Inc., Cranbury, NJ, Manufactured by: Sun Pharmaceuticals, Industries, Ltd., Gujarat, India; a) JKT0075A, JKT0076A, JKT0213A, JKT0215A, JKT0369A, JKT0214A, JKT0368A, JKT0370A exp Jan-20; JKT0371A, JKT0515A, JKT0514A, JKT0516A, JKT0518A, JKT0517A, JKT0694A, JKT0695A, JKT0696A, exp Feb-20; JKT0697A, JKT0698A, JKT1063A, JKT1064A, JKT1065A, JKT1148A, JKT1068A, JKT1146A, JKT1066A exp Mar-20; JKT1149A, JKT1147A, JKT1150A, JKT1427A, JKT1428A, JKT1426A, JKT1429A, JKT1540A, JKT1539A, JKT1541A, JKT1543A, JKT1542A exp Apr-20; JKT1725A, JKT1574A, JKT1727A, JKT1863A, JKT1864A, JKT1865A, JKT1726A exp May-20; JKT2191A exp Jun-20; JKT1866A, JKT2192A, JKT2193A, JKT2194A, JKT2575A, JKT2195A, JKT2576A exp Jul-20; JKT2578A, JKT2579A, JKT2911A, JKT2907A, JKT2908A, JKT2909A, JKT2910A, JKT2577A exp Aug-20; JKT3104A, JKT3105A, JKT3106A, JKT3260A, JKT3261A, JKT3263A, JKT3107A, JKT3467A, JKT3262A, JKT3264A exp Sep-20; JKT3788A, JKT3468A, JKT3749A, JKT3469A, JKT3787A exp Oct-20; JKT3790A, JKT4019A, JKT3789A, JKT4016A, JKT4014A, JKT4017A, Nov-20; JKU0040A exp Dec-20; JKU0041A, JKU0042A, JKU1043A, JKU1044A exp Feb-21; b) JKT1862A, JKT1578A exp May-20; JKT2000A, JKT1999A, JKT2001A exp Jun-20; JKT2593A, JKT2594A exp Jul-20; JKT3863A, JKT4013A exp Nov-20; JKU0037A, JKU0038A, JKU0358A exp Dec-20 | — |
What to do — step by step
Contact Manufacturer
Reach out to Sun Pharmaceutical for details about the recalled vials and any necessary actions.
Questions people ask
Why is this product being recalled?
The product was manufactured under similar conditions to a previously rejected batch that had quality issues.
What should I do if I have this product?
Contact Sun Pharmaceutical for details about the recalled vials and any necessary actions.
Are there specific expiration dates for the recalled vials?
Yes, the recalled vials have specific expiration dates listed in the recall notice.
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-0787-2020 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-0787-2020 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-0787-2020 (January 14, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0787-2020 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.