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Garry N Sun USA Inc. Recall: State of Iowa collected consumer sample and found high levels of lead - 12,200 mg/kg

United States

TerminatedClass I

Company
Garry N Sun USA Inc.
Product
Mahayograj Guggulu; 120 Vegetarian Capsules, 1/2 lb. bags o…
Recall date
May 17, 2021
Terminated
July 2, 2021
Source
FDA

Reason for recall

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

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Mahayograj Guggulu; 120 Vegetarian Capsules, 1/2 lb. bags of powder Dietary Supplement, 1030 Matley Lane, Unit A Reno, NV 89502 Serving size: 2 capsule Servings per container: 60 Proprietary Blend - 500 mg Certified Organic Distributed by Garry N Sun USA Not published in this source record 18 lbs. Lot number #11850, Use by date of 12/31/2023

Distribution

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

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0633-2021
Event ID
87946
Status
Terminated
Classification
Class I
Company
Garry N Sun USA Inc.
Product description
Mahayograj Guggulu; 120 Vegetarian Capsules, 1/2 lb. bags of powder Dietary Supplement, 1030 Matley Lane, Unit A Reno, NV 89502 Serving size: 2 capsule Servings per container: 60 Proprietary Blend - 500 mg Certified Organic Distributed by Garry N Sun USA
Quantity
18 lbs.
Reason
State of Iowa collected consumer sample and found high levels of lead - 12,200 mg/kg
Recall initiation date
May 17, 2021
Report date
June 9, 2021
Classification date
Not published in this source record
Termination date
July 2, 2021
Distribution pattern
North Carolina, Arkansas, Hawaii, Idaho, New Mexico, Texas, Florida, Arizona, Washington, Michigan, California, Canada, Germany.
UPC, lot, and code information
Lot number #11850, Use by date of 12/31/2023
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Garry N Sun USA Inc.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.