D.B.P. Distribution recalls Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC
D.B.P. Distribution recalls Titanium 4000 4000mg capsules due to undeclared sildenafil and tadalafil without FDA approval. No remedy specified in official notice.
Recall notice
Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil.
Contact the company & request your remedy
What happened, in plain English
D.B.P. Distribution recalled Titanium 4000 4000mg capsules because they contain undeclared sildenafil and tadalafil without FDA approval. This poses a risk of serious health issues since these drugs require regulatory approval before sale. Read more at govinfonow.com/recall/38882-titanium-4000-capsules-recalled-for-undeclared-sildenafil-and-tadalafil.
Source Summary by GovInfoNow · govinfonow.com/recall/38882-titanium-4000-capsules-recalled-for-undeclared-sildenafil-and-tadalafil · Updated October 5, 2026 · FDA enforcement record: FDA #D-1292-2019
Cite this page
“Titanium 4000 Capsules Recalled for Undeclared Sildenafil and Tadalafil.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38882-titanium-4000-capsules-recalled-for-undeclared-sildenafil-and-tadalafil. Based on FDA recall #D-1292-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1292-2019%22&limit=1).
Why it’s dangerous
These capsules contain sildenafil and tadalafil without proper FDA approval. This means they could cause serious health problems like heart issues or interactions with other medications.
Who’s affected
Anyone who owns or uses these capsules. People with underlying health conditions or those taking other medications are at higher risk.
How to tell if you have this one
Check for the product name 'Titanium 4000', 4000mg capsules, 30 blister packs, and UPC 86077000020. The expiration date is December 29, 2020.
- Brand
Titanium 4000- Product
Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC- Category
Drug
What to do — step by step
Check Product Details
Look for the product name 'Titanium 4000', 4000mg capsules, 30 blister packs, and UPC 86077000020.
Questions people ask
Why were these capsules recalled?
The capsules contain undeclared sildenafil and tadalafil without FDA approval.
Is there a remedy for these capsules?
The official notice does not specify a remedy.
What is the expiration date for these capsules?
The expiration date is December 29, 2020.
Contact Titanium 4000
We’ve drafted a message you can send Titanium 4000 to request your refund or repair — edit it as you like.
Subject: Recall D-1292-2019 — Titanium 4000 Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distr Hello, I own a Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC that is covered by recall D-1292-2019 from Titanium 4000. 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-1292-2019 (April 23, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1292-2019 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.