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Showing 2441–2460 of 4420 results

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Shredded Tofu (Danshi) – Undeclared Sesame (2025)

Product does not declare allergen ingredient sesame.

Class IHigh

FDAJun 25, 2025Nationwide• Shang Hao Jia, Inc

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

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

Class IIILow

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

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 (Aceto) – Concentration Variance (2025)

4% Lithium Orotate product may only contain 3% and 9% Lithium Orotate product may contain 4.45%

Class IIILow

FDAJun 24, 2025AZ, CA, FL +5 more• Aceto US, L.L.C

Metoprolol Succinate Tablets 25mg (Granules) – Dissolution Specification Failure (2025)

Failed Dissolution Specifications: Product failed to meet dissolution acceptance criteria in the stability studies at the 6th month (25¿C/60% RH) long-term.

Class IIModerate

FDAJun 24, 2025Nationwide• Granules Pharmaceuticals Inc.

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 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 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

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 Capsules (GMP Laboratories) – Manufacturing Specification (2025)

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

Class IIILow

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

LVP Primary Administration Set (Fresenius Kabi) – Cassette Leak (2025)

Potential for external cassette leaks

Moderate

FDAJun 24, 2025Nationwide• Fresenius Kabi USA, LLC

PILLAR SA Ti Implant (Orthofix) – Labeling Discrepancy (2025)

A 37 mm implant width intervertebral body fusion device has a labeling discrepancy with incorrect width of 33 mm stated on the outer label side flap and inner label side flap information box. The 37 mm width on the front labels is correct.

Low

FDAJun 24, 2025Nationwide• Orthofix U.S. LLC

Astra EV Digital Analog (Preat) – Rotational Misalignment (2025)

Due to manufacturing error, digital analog rotational feature is 180 degrees off.

Moderate

FDAJun 24, 2025Nationwide• Preat Corp

XC40 (VOLVO) – Brake System Issue (2025)

Volvo Car USA, LLC (Volvo Car) is recalling certain 2023 Volvo C40 BEV, 2025 EC40, 2023-2024 XC40 BEV, 2020-2026 XC90 PHEV, 2022-2026 XC60 PHEV, 2023-2025 S60 PHEV, 2024-2025 V60 PHEV, and 2025-2026 EX40 and 2025 S90 PHEV vehicles. In certain driving scenarios while coasting down a hill and using "B" mode or "One Pedal Drive," the vehicle may lose brake function.

Moderate

NHTSAJun 24, 2025Nationwide• VOLVO

LVP Blood Products Set (Fresenius Kabi) – Cassette Leak (2025)

Potential for external cassette leaks

Moderate

FDAJun 24, 2025Nationwide• Fresenius Kabi USA, LLC

BD COR System Software (Becton Dickinson) – Functionality Issue (2025)

Potential for functionality issue that supports the Over labeling feature and could lead to possible false negative results.

Low

FDAJun 23, 2025Nationwide• Becton Dickinson & Co.

Mack MD Electric (MACK) – Throttle Communication (2025)

Mack Trucks, Inc. (Mack) is recalling certain 2024-2026 Mack MD vehicles. When the Controller Area Network (CAN) communications are interrupted, the throttle signal from the electro mobility control unit may retain the last known throttle setting, and the engine will not return to idle as intended. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 124, "Accelerator Control Systems."

High

NHTSAJun 23, 2025Nationwide• MACK

HeartMate Power Unit (Thoratec) – Power Cord Locking (2025)

Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which prevents the locking mechanism from properly engaging with the Mobile Power Unit and may cause unintended disconnect.

Moderate

FDAJun 23, 2025Nationwide• Thoratec LLC

Kawasaki W230 (KAWASAKI) – Electrical Ground Connection (2025)

Kawasaki Motors Corp., U.S.A. (KMC) is recalling certain 2025 BJ230A (W230 ABS) motorcycles. The electrical ground connection between the battery and frame may become unstable and result in an engine stall.

High

NHTSAJun 23, 2025Nationwide• KAWASAKI

Keystone Carbon (KEYSTONE) – Gate Pin Issue (2025)

Keystone RV Company (Keystone) is recalling certain 2025 Carbon, Fuzion, and Raptor toy hauler recreational trailers. The rear gate pins and/or leg support bracket may be missing, allowing the gate to shift during operation.

Moderate

NHTSAJun 23, 2025Nationwide• KEYSTONE

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