RECALL RECORD — CLASS IRecall closedF-0633-2021/FDA enforcement

Mahayograj Guggulu

What you need to know

Class I
  • What happened

    State of Iowa collected consumer sample and found high levels of lead - 12, 200 mg/kg

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. Lead is a toxic heavy metal with no safe blood lead level in children.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDADistribution not listedMore supplements

Advertisement

Ad

Know someone who bought this?

A quick share can keep a pantry check from becoming a missed warning.

Match before you discard

Product identification

Source: FDA FOOD

Brand nameGarry N Sun USA INC.
Recalling firmGarry N Sun USA INC.Reno, NV, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot number #11850, Use by date of 12/31/2023
Distribution area

North Carolina, Arkansas, Hawaii, Idaho, New Mexico, Texas, Florida, Arizona, Washington, Michigan, California, Canada, Germany.

Canada, Mexico, Germany

Quantity affected18 lbs.
Recall initiationFDA report date: June 9, 2021
FDA recall numberF-0633-2021

Beyond the headline

The recall, in context

Garry N Sun USA INC. initiated this supplements recall on May 17, 2021. The FDA enforcement report states: State of Iowa collected consumer sample and found high levels of lead - 12, 200 mg/kg. The FDA report lists distribution as: North Carolina, Arkansas, Hawaii, Idaho, New Mexico, Texas, Florida, Arizona, Washington, Michigan, California, Canada, Germany.

The FDA enforcement report describes the reason as: State of Iowa collected consumer sample and found high levels of lead - 12, 200 mg/kg

Mahayograj Guggulu was made or distributed by Garry N Sun USA INC. in Reno, NV, United States. This page reflects FDA report F-0633-2021, dated June 9, 2021.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, lead is a toxic heavy metal with no safe blood lead level in children.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Lead contamination

Possible health effects

Lead can affect the nervous system and is especially harmful to children and pregnant people. Symptoms may include abdominal pain, constipation, fatigue or headaches, but some exposed people have no obvious symptoms.

When symptoms may appear

Health effects depend on the amount and duration of exposure; there is no safe blood lead level in children.

Higher-risk groups

Infants, young children, pregnant people and anyone with repeated exposure are at greatest risk.

What to do now

  1. 1Stop using or eating the affected product and prevent children from handling it.
  2. 2Keep the packaging and ask the retailer or manufacturer about a refund; follow local guidance for safe disposal.
  3. 3If a child or pregnant person may have been exposed, contact a healthcare professional about blood lead testing.

Do not use home remedies or ignore possible exposure; clinical testing is the appropriate next step.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Mahayograj Guggulu recall?

Garry N Sun USA INC. recalled Mahayograj Guggulu in an FDA Class I enforcement action reported as F-0633-2021. State of Iowa collected consumer sample and found high levels of lead - 12, 200 mg/kg

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the affected product and prevent children from handling it. Keep the packaging and ask the retailer or manufacturer about a refund; follow local guidance for safe disposal. If a child or pregnant person may have been exposed, contact a healthcare professional about blood lead testing.

Is the Garry N Sun USA INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0633-2021. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Related alerts

Recent Lead recalls

All alerts

Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.