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Class III: unlikely to cause harmTerminated

GMP Laboratories of America Lithium Orotate Recall

Lithium Orotate, Weyland Brain Nutrition

GMP Laboratories of America Inc · Anaheim, CA

Risk level
Class III
Reported by FDA
Aug 20, 2025
Recall ID
H-0448-2025
Check your lot numberHow we source this data

Summary

GMP Laboratories of America recalled Lithium Orotate starting Jun 24, 2025. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report H-0448-2025 on Aug 20, 2025. Reason: Downstream recall of a dietary supplement ingredient that was manufactured out of specification. Status: Terminated.

Why it was recalled

Downstream recall of a dietary supplement ingredient that was manufactured out of specification.

Product description

Lithium Orotate, Weyland Brain Nutrition ; 60 vegetarian capsules, Dietary Supplement; Distributed by Enjoy Nutirtion, LLC. San Francisco, CA 94108, (415) 894-0537 2.5 mg UPC#: X001SBI13J 5 mg UPC#: X000PY16Z5 10 mg UPC#: X000T9B9B7 20 mg UPC#: X001VBLW8H 1000 MCG UPC#: X003SBV661

Lot numbers, UPCs & expiration codes

2.5mg Lot #: 21166, 21640, 21821, 22281, 22757 Expire date: 11/2025, 09/2026, 05/2027, 02/2028 5 mg Lot#: 21123, 21300, 21498, 21783, 21994, 22218, 22299, 22457, 22718 Expire date: 10/2025, 05/2026, 08/2026, 01/2027, 04/2027, 05/2027, 08/2027, 02/2028 10mg Lot#: 21107, 21181, 21288, 21371, 21499, 21695, 21993, 22105, 22200, 22399, 22556, 22650, 22736 Expire date: 10/2025, 12/2025, 02/2026, 03/2026, 05/2026, 07/2026, 01/2027, 01/2027, 03/2027, 07/2027, 10/2027, 01/2028, 02/2029 20mg Lot#: 21301, 21505, 21911, 22106, 22257, 22397, 22557, 22918 Expire date: 02/2026, 05/2026, 10/2026, 05/2027, 07/2028, 10/2027, 04/2028 1000 MCG Lot#: 21442, 22647 Expire date: 05/2025, 01/2027

Where it was sold

Distribution was to a single customer who received product in California and Oklahoma.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-0448-2025
Classification
Class III
Status
Terminated
Recall initiated
Jun 24, 2025
FDA report date
Aug 20, 2025
Quantity
~185,482 capsules
Recall type
Voluntary: Firm initiated
Recalling firm
GMP Laboratories of America Inc

Original FDA data

Every field from FDA enforcement report H-0448-2025, exactly as published.

Show all FDA fields
City
Anaheim
State
CA
Status
Terminated
Country
United States
Event ID
97158
Address
2931 E La Jolla St
Code information
2.5mg Lot #: 21166, 21640, 21821, 22281, 22757 Expire date: 11/2025, 09/2026, 05/2027, 02/2028 5 mg Lot#: 21123, 21300, 21498, 21783, 21994, 22218, 22299, 22457, 22718 Expire date: 10/2025, 05/2026, 08/2026, 01/2027, 04/2027, 05/2027, 08/2027, 02/2028 10mg Lot#: 21107, 21181, 21288, 21371, 21499, 21695, 21993, 22105, 22200, 22399, 22556, 22650, 22736 Expire date: 10/2025, 12/2025, 02/2026, 03/2026, 05/2026, 07/2026, 01/2027, 01/2027, 03/2027, 07/2027, 10/2027, 01/2028, 02/2029 20mg Lot#: 21301, 21505, 21911, 22106, 22257, 22397, 22557, 22918 Expire date: 02/2026, 05/2026, 10/2026, 05/2027, 07/2028, 10/2027, 04/2028 1000 MCG Lot#: 21442, 22647 Expire date: 05/2025, 01/2027
Postal code
92806-1306
Report date
Aug 20, 2025
Product type
Food
Recall number
H-0448-2025
Classification
Class III
Recalling firm
GMP Laboratories of America Inc
Product quantity
~185,482 capsules
Termination date
Feb 24, 2026
Reason for recall
Downstream recall of a dietary supplement ingredient that was manufactured out of specification.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Lithium Orotate, Weyland Brain Nutrition ; 60 vegetarian capsules, Dietary Supplement; Distributed by Enjoy Nutirtion, LLC. San Francisco, CA 94108, (415) 894-0537 2.5 mg UPC#: X001SBI13J 5 mg UPC#: X000PY16Z5 10 mg UPC#: X000T9B9B7 20 mg UPC#: X001VBLW8H 1000 MCG UPC#: X003SBV661
Distribution pattern
Distribution was to a single customer who received product in California and Oklahoma.
Recall initiation date
Jun 24, 2025
Initial firm notification
Telephone
Center classification date
Aug 8, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0448-2025, published Aug 20, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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