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Schwinnng Herbal Dietary Supplement Capsules recall

FDA recall D-0494-2024 · initiated Apr 22, 2024

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated May 22, 2024How we research

Stop Clopez Corp recalled Schwinnng Herbal Dietary Supplement Capsules in Apr 2024 — an FDA Class I recall (D-0494-2024) because Marketed Without An Approved NDA/ANDA.

Most serious — a reasonable probability that use will cause serious harm or death.

Why it was recalled

Marketed Without An Approved NDA/ANDA

Sold unapproved, or found to contain something undeclared

The product should not have been on sale in this form — often a supplement found to contain a hidden prescription drug.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

Lot 2108; EXP 10/31/2024

Quantity recalled: 5 boxes

Details

Product
Schwinnng Herbal Dietary Supplement Capsules, packaged in 10-count boxes, distributed by VSD Productions Inc., Las Vegas, NV.
Recalling company
Stop Clopez Corp
Classification
Class I
Status
Terminated
Type
Voluntary: Firm initiated
Distribution
Distribution worldwide via amazon.com
Initiated
Apr 22, 2024
FDA report date
May 22, 2024
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Schwinnng Herbal Dietary Supplement Capsules recalled?
Stop Clopez Corp recalled Schwinnng Herbal Dietary Supplement Capsules in Apr 2024 — an FDA Class I recall (D-0494-2024) because Marketed Without An Approved NDA/ANDA. Most serious — a reasonable probability that use will cause serious harm or death.
Why was Schwinnng Herbal Dietary Supplement Capsules recalled?
Per the FDA enforcement record, the reason for recall D-0494-2024 was: Marketed Without An Approved NDA/ANDA
Is a recalled Schwinnng Herbal Dietary Supplement Capsules dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. Most serious — a reasonable probability that use will cause serious harm or death. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Schwinnng Herbal Dietary Supplement Capsules are affected?
Distributed: Distribution worldwide via amazon.com. The recall covers these lots — Lot 2108; EXP 10/31/2024. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0494-2024.

Source: openFDA Drug Enforcement record D-0494-2024

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