S & B Story LLC recalls Imperial Extreme 2000 Capsules, 2000 mg, 1 count blister cards, distributed S&B Shopper LLC. Little Ferry, NJ UPC 7
FDA found tadalafil and sildenafil in unapproved Imperial Extreme 2000 Capsules. Recalled due to lack of FDA approval. No specific remedy stated in recall notice.
Recall notice
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and sildenafil.
Contact the company & request your remedy
What happened, in plain English
S & B Story LLC recalled Imperial Extreme 2000 Capsules (2000 mg) because they contain unapproved medications tadalafil and sildenafil. This poses a risk of serious health effects since the product was not approved by the FDA. Read more at govinfonow.com/recall/36248-s-b-story-imperial-extreme-2000-capsules-recall-unapproved-medication.
Source Summary by GovInfoNow · govinfonow.com/recall/36248-s-b-story-imperial-extreme-2000-capsules-recall-unapproved-medication · Updated October 4, 2026 · FDA enforcement record: FDA #D-0352-2021
Cite this page
“S & B Story Imperial Extreme 2000 Capsules Recall: Unapproved Medication Found.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36248-s-b-story-imperial-extreme-2000-capsules-recall-unapproved-medication. Based on FDA recall #D-0352-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0352-2021%22&limit=1).
Why it’s dangerous
The FDA found tadalafil and sildenafil in the capsules, which are medications not approved for sale in the U.S. These drugs can cause serious health issues if taken without proper medical supervision.
Who’s affected
Anyone who purchased Imperial Extreme 2000 Capsules from S & B Shopper LLC in Little Ferry, NJ. People using these capsules for medical purposes are at higher risk due to unapproved ingredients.
How to tell if you have this one
Check for Imperial Extreme 2000 Capsules with 2000 mg per capsule, 1 count blister cards, distributed by S & B Shopper LLC in Little Ferry, NJ. The product has a UPC code starting with 7 18122 04073 5.
- Brand
S & B Story LLC- Product
Imperial Extreme 2000 Capsules, 2000 mg, 1 count blister cards, distributed S&B Shopper LLC. Little Ferry, NJ UPC 7- Category
Drug
What to do — step by step
Check Product Details
Look for the product name, dosage, and distribution details to confirm if it matches the recalled items.
Questions people ask
Why was this product recalled?
The FDA found tadalafil and sildenafil in the capsules, which are medications not approved for sale in the U.S.
Is there a remedy for this product?
The recall notice does not specify any remedy.
How can I tell if I have the recalled product?
Check for Imperial Extreme 2000 Capsules with 2000 mg per capsule, 1 count blister cards, distributed by S & B Shopper LLC in Little Ferry, NJ, with the UPC code starting with 7 18122 04073 5.
Contact S & B Story LLC
We’ve drafted a message you can send S & B Story LLC to request your refund or repair — edit it as you like.
Subject: Recall D-0352-2021 — S & B Story LLC Imperial Extreme 2000 Capsules, 2000 mg, 1 count blister cards, distributed S&B Sho Hello, I own a Imperial Extreme 2000 Capsules, 2000 mg, 1 count blister cards, distributed S&B Shopper LLC. Little Ferry, NJ UPC 7 that is covered by recall D-0352-2021 from S & B Story LLC. 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-0352-2021 (March 25, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0352-2021 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.