Na Na Collection recalls Triple SupremeZen Gold 3500, Packaged in paper packaging with a pill blister,1 capsule per box, Distributed by VIEW
Na Na Collection recalls Triple SupremeZen Gold 3500 capsules due to FDA finding unapproved drugs tadalafil and sildenafil. Consumers should check product details and contact the manufacturer.
Recall notice
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
Contact the company & request your remedy
What happened, in plain English
Na Na Collection is recalling Triple SupremeZen Gold 3500 capsules because they contain unapproved drugs tadalafil and sildenafil, which the FDA detected. This poses a risk of unintended medication effects since the product was marketed without FDA approval. Read more at govinfonow.com/recall/36228-na-na-collection-triple-supremezen-gold-3500-unapproved-drugs-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/36228-na-na-collection-triple-supremezen-gold-3500-unapproved-drugs-risk · Updated October 4, 2026 · FDA enforcement record: FDA #D-0354-2021
Cite this page
“Na Na Collection Triple SupremeZen Gold 3500: Unapproved Drugs Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36228-na-na-collection-triple-supremezen-gold-3500-unapproved-drugs-risk. Based on FDA recall #D-0354-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0354-2021%22&limit=1).
Why it’s dangerous
The product contains tadalafil and sildenafil without FDA approval. These drugs are prescription medications that can cause serious health issues if used without proper medical supervision.
Who’s affected
Anyone who owns or uses Triple SupremeZen Gold 3500 capsules. People taking these capsules for medical reasons are at higher risk due to potential drug interactions.
How to tell if you have this one
Check for the product name 'Triple SupremeZen Gold 3500', paper packaging with a pill blister, 1 capsule per box, and the UPC 7 15122 05089 4. The lot number is GATCO 1805 with an expiration date of 12/30/2024.
- Brand
Na Na Collection- Product
Triple SupremeZen Gold 3500, Packaged in paper packaging with a pill blister,1 capsule per box, Distributed by VIEW- 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
Ongoing- Distribution
Nationwide with the United States
| Recall number | Product, codes & lots |
|---|---|
| D-0353-2021 | PremierZen Platinum 5000, Packaged in paper packaging with a pill blister, 1 capsule per box, Distributed by New Premier Group Los Angeles CA 90006; Lot #: GATCO 01671, Exp Date 12/30/2024 Serial # 728175421856 |
| D-0354-2021 | Triple SupremeZen Gold 3500, Packaged in paper packaging with a pill blister,1 capsule per box, Distributed by VIEW LIFE Distributors Los Angeles CA 90005 UPC 7 15122 05089 4; Lot #: GATCO 1805, Exp. Date 12/30/2024 Serial # 715122050894 |
What to do — step by step
Check Product Details
Look for the product name 'Triple SupremeZen Gold 3500', paper packaging with a pill blister, 1 capsule per box, and the UPC 7 15122 05089 4.
Questions people ask
Why is this product being recalled?
The FDA found tadalafil and sildenafil in the product, which were marketed without FDA approval.
What should I do if I have this product?
The recall record does not specify a remedy, so check with the manufacturer for further instructions.
Is this product safe to use?
No, the product contains unapproved drugs that could cause serious health issues without medical supervision.
Contact Na Na Collection
We’ve drafted a message you can send Na Na Collection to request your refund or repair — edit it as you like.
Subject: Recall D-0354-2021 — Na Na Collection Triple SupremeZen Gold 3500, Packaged in paper packaging with a pill blister,1 cap Hello, I own a Triple SupremeZen Gold 3500, Packaged in paper packaging with a pill blister,1 capsule per box, Distributed by VIEW that is covered by recall D-0354-2021 from Na Na Collection. 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-0354-2021 (March 30, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0354-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.