Super Panther 7K Capsules Recall: FDA Finds Tainted with Sildenafil and Tadalafil
FDA recalls Super Panther 7K Capsules 1250 mg blend due to contamination with sildendafil and tadalafil. Consumers should not use these products as they pose health risks.
Stop using this now
Marketed without an Approved NDA/ANDA;FDA analysis found product to be tainted with sildendafil and tadalafil
Contact the company
What happened, in plain English
Chiavna Saffron is recalling Super Panther 7K Capsules 1250 mg blend because the FDA found them contaminated with sildendafil and tadalafil. These capsules could cause health risks if taken. Read more at govinfonow.com/recall/41432-super-panther-7k-capsules-recall-fda-finds-tainted-with-sildenafil.
Source Summary by GovInfoNow · govinfonow.com/recall/41432-super-panther-7k-capsules-recall-fda-finds-tainted-with-sildenafil · Updated October 7, 2026 · FDA enforcement record: FDA #D-1145-2017
Cite this page
“Super Panther 7K Capsules Recall: FDA Finds Tainted with Sildenafil and Tadalafil.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41432-super-panther-7k-capsules-recall-fda-finds-tainted-with-sildenafil. Based on FDA recall #D-1145-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1145-2017%22&limit=1).
Why it’s dangerous
The capsules were found to contain sildendafil (sildenafil) and tadalafil, which are prescription medications. Taking these contaminated capsules could lead to unintended health effects due to their active ingredients.
Who’s affected
People who purchased Super Panther 7K Capsules 1250 mg blend from the listed UPC numbers or distribution channels are affected. Those who have taken the capsules are at risk of health issues.
How to tell if you have this one
Check for Super Panther 7K Capsules 1250 mg blend with UPC# 6015577513247 (blister packs in boxes of 30) or UPC# 601577513209 (6-count bottles).
- Brand
Chiavna Saffron- Product
Super Panther 7K Capsules 1250 mg blend, a) 1 count blister cards shipped in boxes of 30 (UPC# 6015577513247); and b) 6- Category
Drug
What to do — step by step
Stop Using Now
Immediately stop using the recalled Super Panther 7K Capsules 1250 mg blend as they contain prescription drugs that could cause health risks.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 8 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest drug recalls
Keep exploring
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-1145-2017 (July 21, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1145-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.