Sun Pharmaceutical Industries, Inc. recalls Sumatriptan Succinate Tablets, 100 mg packaged in 9 (1X9) Unit-of-use blister card, (62756-0522-69), Rx only, Sun
Sun Pharmaceutical recalls 100mg Sumatriptan tablets due to impurities. These prescription migraine meds may have harmful substances that could cause health issues. Check your blister packs for the specific lot numbers listed.
Lower-risk recall
Failed Impurities/Degradation Specifications; out-of-specification results obtained for related substance.
Contact the company & request your remedy
What happened, in plain English
Sun Pharmaceutical is recalling 100mg Sumatriptan Succinate tablets that may contain harmful impurities. This could pose health risks to people using these prescription migraine medications. Read more at govinfonow.com/recall/37491-sun-sumatriptan-100mg-tablets-recall-impurities-may-cause-harm.
Source Summary by GovInfoNow · govinfonow.com/recall/37491-sun-sumatriptan-100mg-tablets-recall-impurities-may-cause-harm · Updated October 5, 2026 · FDA enforcement record: FDA #D-0660-2020
Cite this page
“Sun Sumatriptan 100mg Tablets Recall: Impurities May Cause Harm.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37491-sun-sumatriptan-100mg-tablets-recall-impurities-may-cause-harm. Based on FDA recall #D-0660-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0660-2020%22&limit=1).
Why it’s dangerous
The tablets failed quality tests for impurities and degradation. This means they may contain harmful substances that could cause health problems when taken.
Who’s affected
Prescription migraine sufferers who have the specific 100mg Sumatriptan tablets with the listed lot numbers. People using these medications for migraines are most at risk.
How to tell if you have this one
Check for the 100mg Sumatriptan Succinate tablets in 9-count blister packs with lot numbers 62756-0522-69, JKT4174A (exp. 11/2021), JKU0622A (exp. 01/2022), or JKU1308A (exp. 02/2022).
- Brand
Sun- 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 to 96 distributors and 1 repacker/relabeler.
| Recall number | Product, codes & lots | Quantity | NDC |
|---|---|---|---|
| D-0659-2020 | Sumatriptan Succinate Tablets, 50 mg, packaged in a) 9 (1x9) Unit-of use blister card (NDC 62756-521-69) and b) 100 count bottles, (NDC 62756-521-88), Rx only, Sun Pharma, Cranbury, NJ; a) JKU1939A, JKU1940A, JKU1940B, exp. date 04/2022 and b) JKT4175A, exp. date 11/2020 | 384/100 count bottles | 62756-520-83, 62756-520-88, 62756-520-08, 62756-520-18, 62756-520-69, 62756-520-93, 62756-520-01, 62756-521-83, 62756-521-88, 62756-521-08, 62756-521-18, 62756-521-69, 62756-521-93, 62756-521-01, 62756-522-83, 62756-522-88, 62756-522-08, 62756-522-18, 62756-522-69, 62756-522-93, 62756-522-01 |
| D-0660-2020 | Sumatriptan Succinate Tablets, 100 mg packaged in 9 (1X9) Unit-of-use blister card, (62756-0522-69), Rx only, Sun Pharma, Cranbury, NJ; JKT4174A, exp. date 11/2021 JKU0622A, exp. date 01/2022 JKU1308A, exp. date 02/2022 | 207,585 blisters | — |
What to do — step by step
Check Your Medication
Look for the specific lot numbers listed in the recall notice on your blister pack.
Questions people ask
Why is this medication being recalled?
The tablets failed quality tests for impurities and degradation, meaning they may contain harmful substances.
How can I tell if I have the recalled medication?
Check for the 100mg Sumatriptan Succinate tablets in 9-count blister packs with lot numbers 62756-0522-69, JKT4174A (exp. 11/2021), JKU0622A (exp. 01/2022), or JKU1308A (exp. 02/2022).
What should I do if I have the recalled medication?
The recall notice does not specify a remedy, so you should check with your healthcare provider or pharmacist for advice.
Contact Sun
We’ve drafted a message you can send Sun to request your refund or repair — edit it as you like.
Subject: Recall D-0660-2020 — Sun Sun Hello, I own a Sun that is covered by recall D-0660-2020 from Sun. 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-0660-2020 (December 26, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0660-2020 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.