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Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Enjoy Nutrition, LLC; dba Weyland Brain Nutrition Recalls

All product recalls associated with Enjoy Nutrition, LLC; dba Weyland Brain Nutrition.

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Recall Summary

Total Recalls

1000

Past Year

567

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 341–360 of 7756 recalls

Lithium Orotate 10MG (Enjoy Nutrition) – Potency Issue (2025)

Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.

Class IIILow

FDAJun 24, 2025Nationwide• Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Lithium Orotate 5MG (Enjoy Nutrition) – Potency Issue (2025)

Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.

Class IIILow

FDAJun 24, 2025Nationwide• Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Lithium Orotate Capsules (GMP Laboratories) – Manufacturing Specification (2025)

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

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Class IIILow

FDAJun 24, 2025CA, IN, OK• GMP Laboratories of America Inc

Lithium Orotate 1MG (Enjoy Nutrition) – Potency Issue (2025)

Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.

Class IIILow

FDAJun 24, 2025Nationwide• Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Lithium Orotate Supplement (Weyland Brain) – Potency Mismatch (2025)

Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.

Class IIILow

FDAJun 24, 2025Nationwide• Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Lithium Orotate 2.5MG (Enjoy Nutrition) – Potency Issue (2025)

Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.

Class IIILow

FDAJun 24, 2025Nationwide• Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

SIGMA Spectrum Pump (Baxter) – Software Version (2025)

Certain Spectrum infusion pumps may have an incorrect version of software.

FDAJun 20, 2025CA, FL, IL +7 more• Baxter Healthcare Corporation

Natus Brain Monitor Breakout Box (Natus) – Labeling Error (2025)

Natus received two complaints of left side labeling show impedance for right side.

FDAJun 18, 2025CA, IN, MO +4 more• Natus Neurology DBA Excel Tech., Ltd. (XLTEK)

Estrone RIA (Beckman Coulter) – BSA Lot Variation (2025)

A specific lot of bovine serum albumin (BSA) used for manufacturing of coated tubes (CT) that are included in the Estrone RIA kit lots caused different affinity of manufactured coated tubes to patient samples, causing falsely increased assay results for the impacted Estrone RIA kits.

FDAJun 12, 2025NC• Beckman Coulter Inc.

Torflex Transseptal Sheath Kit (Boston Scientific) – Sterile Barrier Compromise (2025)

Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis in worst case scenario. Potential punctures may go undetected in clinical settings due to small size and variable location.

FDAJun 10, 2025Nationwide• Boston Scientific Corporation

VersaCross RF Wire (Boston Scientific) – Sterile Barrier Compromise (2025)

FDAJun 10, 2025Nationwide• Boston Scientific Corporation

VersaCross Access Solution (Boston Scientific) – Sterile Barrier Compromise (2025)

FDAJun 10, 2025Nationwide• Boston Scientific Corporation

VersaCross Transseptal Sheath Kit (Boston Scientific) – Sterile Barrier Compromise (2025)

FDAJun 10, 2025Nationwide• Boston Scientific Corporation

BostonSight PROSE Lens (Boston Foundation For Sight) – Lens Dimension Error (2025)

Select orders of lenses were manufactured with errors impacting sagittal height, haptics, or both.

FDAJun 10, 2025Nationwide• Boston Foundation For Sight

BostonSight Scleral Lens (Boston Foundation For Sight) – Lens Dimension Error (2025)

Select orders of lenses were manufactured with errors impacting sagittal height, haptics, or both.

FDAJun 10, 2025Nationwide• Boston Foundation For Sight

Superion IDS Kit (Boston Scientific) – Performance Consistency Issue (2025)

As a result of a comprehensive product performance review it was determine that the device and instruments are not consistently meeting expected performance levels. Issues include breakage of the instruments and implant/device.

FDAJun 6, 2025Nationwide• Boston Scientific Neuromodulation Corporation

Battle Motors LET2 (Battle Motors) – Steering Nut Problem (2025)

Battle Motors, Inc. (Battle Motors) is recalling certain 2024-2025 Let2 trucks. The steering wheel retaining nut may have been improperly tightened, allowing the steering wheel to loosen and detach from the steering shaft.

NHTSAJun 2, 2025Nationwide• BATTLE MOTORS

Platelia Toxo IgM (Bio-Rad) – False Positive Results (2025)

Due to a risk of false positive results that could lead to unnecessary medical treatment.

FDAMay 30, 2025Nationwide• Bio-Rad Laboratories, Inc.

Hillrom Q-Link 13 Component (Baxter Healthcare) – False Attachment Risk (2025)

The Q-link 13 could allow for an improper attachment (false latching) of the Quick-Release Hook used on Sling Bars and other accessories. This could result in a critical injury from a patient fall as the false latched component may initially bear weight but can loosen from the Q-link resulting in a detachment and drop.

FDAMay 30, 2025Nationwide• Baxter Healthcare Corporation

Inseego USB8 4G Dongle Kit (Remote Diagnostic) – Outdated Software (2025)

Kit USB flash drive contains outdated software, which could result in reverting patient monitor to outdated software and reintroducing the video laryngoscope issue (related to an August 2023 recall), which could lead to delay in diagnosis, delayed treatment, hypoxia due to unexpected loss of video laryngoscopy and all other monitor measurements during system restart.

FDAMay 30, 2025Nationwide• Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom