Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

Home
/
Brands
/
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.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

295

Class I (Serious)

116

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 141–160 of 4465 recalls

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.

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.

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

Choco Mousse (SABORES FIT BAKERY) – undeclared allergens (2025)

Undeclared Allergen

1...6 789 10...224

Page 8 of 224Next

Undeclared allergens: Milk, Eggs, Soy Ingredients (Soybean oil, Soy Lecithin), Wheat, Tree Nuts (Almonds, Hazelnuts) on label and incomplete Contains statement

Class IHigh

FDAJun 17, 2025FL• SABORES FIT BAKERY

Four Milk Mousse (SABORES FIT BAKERY) – undeclared allergens (2025)

Undeclared Allergen

Undeclared allergens: Milk, Eggs, Soy Ingredients (Soybean oil, Soy Lecithin), Wheat, Tree Nuts (Almonds, Hazelnuts) on label and incomplete Contains statement

FDAJun 17, 2025FL• SABORES FIT BAKERY

Passion Fruit Mousse (SABORES FIT BAKERY) – undeclared allergens (2025)

Undeclared Allergen

Undeclared allergens: Milk, Eggs, Soy Ingredients (Soybean oil, Soy Lecithin), Wheat, Tree Nuts (Almonds, Hazelnuts) on label and incomplete Contains statement

FDAJun 17, 2025FL• SABORES FIT BAKERY

Strawberry Mousse (SABORES FIT BAKERY) – undeclared allergens (2025)

Undeclared Allergen

Undeclared allergens: Milk, Eggs, Soy Ingredients (Soybean oil, Soy Lecithin), Wheat, Tree Nuts (Almonds, Hazelnuts) on label and incomplete Contains statement

FDAJun 17, 2025FL• SABORES FIT BAKERY

Three Milk Mousse (SABORES FIT BAKERY) – undeclared allergens (2025)

Undeclared Allergen

Undeclared allergens: Milk, Eggs, Soy Ingredients (Soybean oil, Soy Lecithin), Wheat, Tree Nuts (Almonds, Hazelnuts) on label and incomplete Contains statement

FDAJun 17, 2025FL• SABORES FIT BAKERY

Sodium Chloride Injection (B Braun) – Sterility Compromise (2025)

Lack of assurance of sterility: pinholes, within the finger boxes used during Form Fill Seal process resulting in leaks.

Class IIModerate

FDAJun 16, 2025Nationwide• B BRAUN MEDICAL INC

Akreos Intraocular Lens (Bausch & Lomb) – Diopter Calculation Error (2025)

An off-power error was identified, which resulted in a diopter of 16, rather than the intended 3 diopter. Implantation of affected intraocular lens could result in functional visual impairment or reduction in visual acuity which could result in the need for optical or surgical correction.

FDAJun 6, 2025AZ, CA• Bausch & Lomb Surgical, Inc.

Azurion 7 M20 X-Ray (Philips Medical) – Gearbox Bolt Loosening (2025)

Potential for bolts connecting the gearbox to the mounting flange of the C-arm to become loose.

FDAJun 4, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

BD FACS Setup Beads (Becton Dickinson) – Spectral Overlap Error (2025)

Due to customer complaints, errors in spectral overlap factors table for 7-color setup beads may affect accurate setup of the flow cytometry instrument prior to analyzing samples.

FDAJun 3, 2025AZ, AR, CA +34 more• Becton, Dickinson and Company, BD Bio Sciences

BD FACS Setup Beads (Becton Dickinson) – Spectral Overlap Error (2025)

Due to customer complaints, errors in spectral overlap factors table for 7-color setup beads may affect accurate setup of the flow cytometry instrument prior to analyzing samples.

FDAJun 3, 2025AZ, AR, CA +34 more• Becton, Dickinson and Company, BD Bio Sciences

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.

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

Gamma4 Right Long Nail (Stryker) – Incorrect Nail Geometry (2025)

Investigation confirmed that the GAMMA4 Right Long Nail was manufactured with the geometry of a left nail.

FDAMay 28, 2025Nationwide• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

Azurion R1.x and R2.x Systems (Philips) – Communication Software Issue (2025)

Laceration Risk

A software issue was identified in the internal communication process between the system software and the X-ray generator firmware. Loss of imaging (X-ray) functionality caused by the software issue in either of the two situations identified could result in a delay of therapy. The potential delay may result in serious adverse health outcomes, including the possibility of death, especially when the system is used with patients undergoing complex and/or urgent interventions for potentially life-threatening conditions (e.g., acute ischemic stroke, ST-segment elevation myocardial ischemia, life-threatening bleedings).

FDAMay 28, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

O-arm O2 Imaging System (Medtronic) – Gantry Support Damage (2025)

A mechanical component that supports the O2 gantry to the support structure in affected devices may have been damaged during manufacture.

FDAMay 27, 2025Nationwide• Medtronic Navigation, Inc.-Boxborough

Femoral Nail T2 GTN (Stryker) – Incorrect Nail Version (2025)

Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but contained a left nail.

FDAMay 22, 2025Nationwide• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

Femoral Nail T2 GTN (Stryker) – Incorrect Nail Version (2025)

Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but contained a left nail.

FDAMay 22, 2025Nationwide• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

Bigfoot Unity Diabetes System (Bigfoot) – Insulin Pen Error (2025)

Due to a software/firmware issue diabetes management system may provide a device error and cause the insulin pen to become unresponsive and unable to function. This error may pose a potential health risk for people living with diabetes as they may not have all information necessary to make a timely treatment decision.

FDAMay 21, 2025Nationwide• BIGFOOT BIOMEDICAL