FDA recall record

Ultra Supplement SUSTANGO recall — FDA D-1350-2022

Marketed Without an Approved NDA/ANDA: Analytical testing showed the presence of tadalafil.

Class Iclassification
D-1350-2022official record ID
Aug 10, 2022report date

Recall record at a glance

Official recordD-1350-2022
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmUltra Supplement LLC
Report dateAug 10, 2022
Recall initiation dateJul 21, 2022
Quantity750 cartons
LocationWilmington, DE, United States

Official product description

SUSTANGO (Pendenadril Tytrate Blend) Capsules, 400 mg, 10-count blisters per carton, Formulated by: Male FX Labs, Bangor, ME, ASIN X0024468I9.

Why the product was recalled

Marketed Without an Approved NDA/ANDA: Analytical testing showed the presence of tadalafil.

Distribution information

Product was distributed nationwide in the USA via Amazon Marketplace on www.amazon.com.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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