UnratedDrug recall · FDA · Published February 8, 2022
MAC DADDY RED Capsules Recall: Unapproved Drugs Contain Tadalafil/Sildenafil
ABC Sales 1 Inc recalls MAC DADDY RED Capsules (10-count blisters) due to unapproved ingredients. These capsules contain undeclared tadalafil and sildenafil, which are FDA-approved for male sexual enhancement but were not properly approved for this product.
Marketed Without An Approved NDA/ANDA: product was found to contain undeclared tadalafil and/or sildenafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making these unapproved drugs.
Take action
Contact the company
📍Recalling firmABC Sales 1 Inc116 Adar Ct · Monsey, NY 10952-3361
“MAC DADDY RED Capsules Recall: Unapproved Drugs Contain Tadalafil/Sildenafil.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35229-mac-daddy-red-capsules-recall-unapproved-drugs-contain-tadalafil-sildenafil. Based on FDA recall #D-0562-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0562-2022%22&limit=1).
The Food and Drug Administration announced on February 8, 2022, that ABC Sales 1 Inc is recalling MAC DADDY RED Capsules because they contain undeclared tadalafil and/or sildenafil. The agency classified the recall as Class I.
How to tell if you have it
Brand: ABC Sales 1 Inc
Product: MAC DADDY RED Capsules
Packaging: 10-count blisters per carton
ASIN: B07TLDZLY2
UPC: 742137 605191
Lot #: 1230004
Expiration date: 03/30/2024
Quantity: 565 cartons
The hazard
The product was found to contain undeclared tadalafil and/or sildenafil, which are ingredients found in FDA-approved products for the treatment of male sexual enhancement. This makes these unapproved drugs.
Context
GovInfoNow's records show ABC Sales 1 Inc has been involved in previous recalls of similar products. Other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15), Buy-Herbal Kian Pee Wan Capsules Recall (2026-03-21), and SUN PHARMACEUTICAL Xyvona 3mg Tablets Recall (2026-05-22).
How to tell if you have this one
Check for MAC DADDY RED Capsules in 10-count blister packs with ASIN B07TLDZLY2 and UPC 742137 605191. The lot number is 1230004 and the expiration date is 03/30/2024.
Brand
ABC Sales 1 Inc
Product
MAC DADDY RED Capsules, packaged in 10-count blisters per carton, ASIN B07TLDZLY2, UPC 742137 605191
Category
Drug
FDA recall event · 2 products
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 I
Status
Terminated
Distribution
Product was distributed nationwide in the USA via Amazon Marketplace.
Recall number
Product, codes & lots
Quantity
D-0562-2022
MAC DADDY RED Capsules, packaged in 10-count blisters per carton, ASIN B07TLDZLY2, UPC 742137 605191.; Lot # 1230004, Exp. date 03/30/2024
565 cartons
D-0563-2022
MAC DADDY PURPLE Capsules, packaged in 10-count blisters per carton, ASIN B08Z63Z4QK, UPC 742137 605764.; Lot # 1230005, Exp. date 03/30/2024
336 cartons
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the product's ASIN B07TLDZLY2 and UPC 742137 605191 on the packaging to confirm it's the recalled item.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Product was distributed nationwide in the USA via Amazon Marketplace.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 24 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0562-2022 (February 8, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0562-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.