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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

442

Class I (Serious)

138

Most Recent

Dec 2025

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 241–260 of 7663 recalls

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

Pinon Coffee (New Mexico Pinon) – Inconsistent Seal (2025)

Clear coat seal on the lid of the single serve cups did not get applied consistently to all cups in the production run. This resulted in the food safe ink printing on some cups to run when exposed to high temperature, high-pressure water used in a K-cup machine.

Class IIILow

FDAJun 20, 2025Nationwide• CinFranky LLC dba New Mexico Pinon Coffee

Portable X-ray System (Digimed) – Minimum Distance Concern (2025)

1...11 121314 15...384

Page 13 of 384Next

Some DIOX-602 units currently in use within the United States do not meet the minimum SSD requirement of 18 cm.

Low

FDAJun 19, 2025Nationwide• DIGIMED CO., LTD 401, 402, 406~411-ho, A-dong 101, Gasan digital 2-ro, Geumcheon-Gu Seoul Korea (the Republic of)

Bardex Lubri-Sil Catheter (C.R. Bard) – Drainage Obstruction (2025)

Laceration Risk

Foley catheter may have an obstructed lumen, which may result in an inability to drain the bladder, of urine and may include pelvic or abdominal pain, flank pain, bladder dysfunction, obstructive uropathy, acute kidney injury and/or hydronephrosis.

High

FDAJun 18, 2025Nationwide• C.R. Bard Inc

KWIK-STIK and LYFO DISK (Microbiologics) – Culture Media Mismatch (2025)

Affected products contain Staphylococcus epidermidis instead of the expected Brevundimonas diminuta. This may cause the user's quality control to fail and delayed diagnosis for the patient.

Low

FDAJun 17, 2025OH, UT• Microbiologics Inc

Chocolate Nonpareils (Wegmans) – undeclared milk (2025)

Undeclared Milk

Undeclared milk

Class IIModerate

FDAJun 16, 2025DE, IN, MD +7 more• Mellace Family Brands California Inc

Mercedes-Benz GLC 300 (Mercedes-Benz) – Headlight Cap Missing (2025)

Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2023 GLC 300 and GLC 300 4MATIC vehicles. The headlights are missing adjustment prevention caps, which can allow the headlights to be improperly adjusted. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."

High

NHTSAJun 11, 2025Nationwide• MERCEDES-BENZ

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.

High

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

Mercedes-Benz GLC 300 (Mercedes-Benz) – Structural Body Concern (2025)

Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2023-2025 GLC 300, GLC 300 4MATIC, 2024-2025 AMG GLC 43 4MATIC, 2025 GLC 350E 4MATIC, and AMG GLC 63 S E vehicles equipped with a panoramic sunroof. In certain crash scenarios, where the rear occupant's head contacts the C-pillar, the pillar may not absorb an adequate amount of the impact. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 201, "Occupant Protection in Interior Impact."

High

NHTSAJun 6, 2025Nationwide• MERCEDES-BENZ

Mercedes-Benz EQS 450+ (Mercedes-Benz) – Pedestrian Alert Issue (2025)

Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2022-2025 S-Class, EQE SUV, EQE, EQS SUV and EQS vehicles. Please see the recall report for a complete list of models. Software in the Acoustic Vehicle Alerting System (AVAS) may cause an incorrect external pedestrian warning sound while reversing. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 141, "Minimum Sound Requirements for Hybrid Electric Vehicles."

High

NHTSAJun 5, 2025Nationwide• MERCEDES-BENZ

Apollo Smoke and CO Detectors (Apollo America) – Alert Failure (2025)

Fire/Burn Risk

This recall involves Apollo America Combination Smoke and Carbon Monoxide Detectors with model number 51000-600. The recalled detector was sold in a white color. The front of the recalled detector has the text "Replace by" followed by a date ranging from 2034/June to 2034/October. "Apollo" and the model number 51000-600 are on the back of the detector. Note: If you choose to dispose of the detector's primary/non-rechargeable lithium battery, do not throw the battery in the trash, or in the general recycling stream (e.g., street-level or curbside recycling bins). Lithium batteries must be disposed of differently than other batteries, because they present a greater risk of fire. Your municipal household hazardous waste (HHW) collection center or battery recycling boxes found at various retail and home improvement stores may accept this lithium battery for disposal. Before taking your battery to a HHW collection center, contact that office ahead of time and ask whether it accepts lithium batteries. If it does not, contact your municipality for further guidance.

Very High

CPSCJun 5, 2025Nationwide• Apollo America Inc., of Auburn Hills, Michigan

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.

High

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

BD Heyman Follower Straight Tip (C.R. Bard) – Catheter Size Incorrect (2025)

Cather packaging may contain the incorrect French size.

Moderate

FDAJun 3, 2025Nationwide• C.R. Bard Inc

Bard Urologist's Tray (C.R. Bard) – Catheter Size Incorrect (2025)

Cather packaging may contain the incorrect French size.

Moderate

FDAJun 3, 2025Nationwide• C.R. Bard Inc

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.

Moderate

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.

Moderate

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

BD Heyman Follower Coude Tip (C.R. Bard) – Catheter Size Incorrect (2025)

Cather packaging may contain the incorrect French size.

Moderate

FDAJun 3, 2025Nationwide• C.R. Bard Inc

Ford F-550 (Custom Truck) – Electrical Node Failure Risk (2025)

Fire/Burn Risk

Custom Truck and Body Works (Custom Truck) is recalling certain 2020 Ford F-550 vehicles equipped with Weldon 8X16 Input-Output nodes. In the event of a short circuit or wiring failure, the firmware in the node may fail to shut off the output pin, resulting in overloaded electrical circuits.

High

NHTSAJun 2, 2025Nationwide• CUSTOM TRUCK & BODY WORKS

Mercedes-Benz GLE 350 4MATIC (Mercedes-Benz) – Mirror Visibility Problem (2025)

Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2024 GLE 350 4MATIC, 2025 GLE 450e 4MATIC, GLE 450 4MATIC Coupe, GLE 450 4MATIC, GLS 450 4MATIC, Maybach GLS 600 4MATIC, AMG GLE 53 4MATIC, AMG GLE 53 4MATIC Coupe, AMG GLE 63 S 4MATIC Coupe, and AMG GLS 63 4MATIC vehicles. The multi-purpose camera and the rearview mirror may be insufficiently attached to the windshield and may detach.

High

NHTSAMay 30, 2025Nationwide• MERCEDES-BENZ

Servo-u MR Ventilator (Maquet) – Patient Circuit Test Error (2025)

Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.

Moderate

FDAMay 30, 2025Nationwide• Maquet Critical Care AB Rontgenvagen