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Neptune Resources, LLC

Neptune Resources, LLC Recalls

All product recalls associated with Neptune Resources, LLC.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 4441–4460 of 37665 recalls

Neptune's Fix Tianeptine Elixir (Neptune Resources) – Unapproved Drug (2024)

Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.

Class IHigh

FDAJan 12, 2024Nationwide• Neptune Resources, LLC

Organic Trek Mix (Woodstock Farms) – Foreign Material (2024)

Product contains stem / vegetation foreign material.

Class IIModerate

FDAJan 12, 2024MD, MA, OR• United Natural Trading Inc. dba Woodstock Farms

Neptune's Fix Tianeptine Elixir (Neptune Resources) – Unapproved Drug (2024)

Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.

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Class I

High

FDAJan 12, 2024Nationwide• Neptune Resources, LLC

Neptune's Fix Tianeptine Tablets (Neptune Resources) – Unapproved Drug (2024)

Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.

Class IHigh

FDAJan 12, 2024Nationwide• Neptune Resources, LLC

Chocolate Fruit & Nut Mix (Woodstock Farms) – Foreign Material (2024)

Product contains stem / vegetation foreign material.

Class IIModerate

FDAJan 12, 2024MD, MA, OR• United Natural Trading Inc. dba Woodstock Farms

Colonoscope PCF-H180AL (Olympus) – Adhesive Deficiency (2024)

Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in temperature or severe shock loads.

Moderate

FDAJan 11, 2024Nationwide• Olympus Corporation of the Americas

Apollo Onyx Delivery Microcatheter (Micro Therapeutics) – Indications Mismatch (2024)

European version of microcatheter were distributed within US which contain a different "Indications for Use".

Low

FDAJan 11, 2024Nationwide• Micro Therapeutics, Inc.

Altec Aerial Device (Altec) – Electrical Cable Problem (2024)

Fire/Burn Risk

Altec Industries, Inc. (Altec) is recalling certain 2004-2023 AT Series aerial devices. The cables in the engine compartment may contact the vehicle's hood, damaging the cables and causing a short circuit.

High

NHTSAJan 11, 2024Nationwide• ALTEC

Colonoscope CF-Q180AL (Olympus) – Adhesive Deficiency (2024)

Moderate

FDAJan 11, 2024Nationwide• Olympus Corporation of the Americas

Colonoscope PCF-Q180AL (Olympus) – Adhesive Deficiency (2024)

Moderate

FDAJan 11, 2024Nationwide• Olympus Corporation of the Americas

Furniture Tip Restraints (New Age) – Safety Risk (2024)

This recall involves plastic New Age furniture tip restraint kits that were sold and distributed by various furniture companies with clothing storage units. Participating Furniture Companies American Drew American Woodcrafters Amini Innovation Corporation Ashley Furniture Industries, LLC Aspenhome Austin Group Furniture, LLC Avalon International Inc., LLC Bassett Furniture Industries, Inc. Drew and Jonathan by Hooker Furnishings Emery Park FD Home Corp. Flexsteel Industries, Inc. Furniture Values International, LLC Homelegance USA, LLC Hooker Furnishings Kincaid Furniture LC Direct Furniture Legacy Classic/Modern Furniture Liberty Furniture Industries, Inc. Magnussen Home Furnishings, Inc. New Classic Home Furnishings, Inc. Parker House Furniture Progressive Furniture Pulaski Furniture Riverside Furniture Samuel Lawrence Springhill Designs Standard Furniture Manufacturing Co., LLC Universal Furniture Van Thiel & Co. Vanguard Furniture Company. The New Age tip restraint kits included a plastic zip-tie, two brackets, and two screws and were sold with clothing storage units manufactured in Vietnam. The date of manufacture should be listed on a sticker or stamped on the clothing storage unit as November 2019 or later. The packaging of the recalled tip kits is white with black lettering and includes directions on how to anchor furniture. The bottom of the packaging states "Manufactured by New Age Industries."

High

CPSCJan 11, 2024Nationwide• New Age Industries Co. LTD, of Vietnam

Evaporator Coil Drain Pans (Daikin) – incorrect marking (2024)

Fire/Burn Risk

This recall expansion includes certain units manufactured between January 2019 and February 2020 that were incorrectly marked. DCT recently discovered that a limited number of evaporator coils that were manufactured during that time frame were incorrectly marked with a 2018 serial number, indicating that the unit was manufactured in 2018. The recall scope now includes about 3,600 additional units with the following configurations and coil serial numbers, as shown in the table below: Type Coil Configuration Affected Furnace Brands Affected Coil Serial Numbers Dates Sold Condensing furnace system Up-Flow (Coil above Furnace) All Prefixes ranging from 1901 through 2101 and certain prefixes ranging from 1811-1812 Jan. 2019 through Nov. 2021 Non-condensing furnace system (Certain configurations) Up-Flow (Coil above Furnace) Any "competitor" brand (excludes Goodman, Daikin or Amana branded furnaces) Prefixes ranging from 1901 through 2101 and certain prefixes ranging from 1811-1812 Jan. 2019 through Nov. 2021. NOTE: Furnace systems that were repaired with a new evaporator coil drain pan between January 2019 and November 2021, with the serial number range listed above, are also included in this recall. Whether a non-condensing furnace system falls within the scope of the recall depends on the location of the burners, which, if unknown, can be verified through DCT's model verification tool at: https://www.recallrtr.com/drainpan. Affected units can be identified through serial numbers found on the evaporator coil or the case, which sits atop the vertically installed furnace. The furnace brand and model number can be found on the furnace on the "Energy Guide" label. Consumers can refer to the instructions on Goodman's model verification tool at: https://www.recallrtr.com/drainpan. The model number of the outdoor condenser may also be required and can be found on a label attached to the product.

High

CPSCJan 11, 2024Nationwide• Daikin Comfort Technologies Manufacturing L.P. (f/k/a Goodman Manufacturing Company L.P.) of Houston, Texas

Vasostrict (Par Sterile Products) – Superpotent Drug (2024)

Superpotent Drug: Assay from the 3-month and 6-month stability intervals exceeded the upper specification limit.

Class IIModerate

FDAJan 11, 2024Nationwide• Par Sterile Products LLC

Rifampin Capsules (Amerisource) – Failed Impurities (2024)

Failed Impurities/Degradation Specification.

Class IIModerate

FDAJan 11, 2024Nationwide• Amerisource Health Services LLC

Colonoscope CF-H180AL (Olympus) – Adhesive Deficiency (2024)

Moderate

FDAJan 11, 2024Nationwide• Olympus Corporation of the Americas

Colonoscope CF-HQ190I (Olympus) – Adhesive Deficiency (2024)

Moderate

FDAJan 11, 2024Nationwide• Olympus Corporation of the Americas

Western Star 6900 (Western Star) – Parking Brake Defect (2024)

Daimler Trucks North America, LLC (DTNA) is recalling certain 2023 Western Star 4900 and Western Star 6900 vehicles. A defect in the inversion valve may delay park brake engagement, which could allow the vehicle to move unintentionally. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 121, "Air Brake Systems."

High

NHTSAJan 10, 2024Nationwide• WESTERN STAR

Synapse PACS v7.3.000 (Fujifilm) – Measurement Error (2024)

Measurements on a Secondary Capture 2D image, that does not have pixel spacing in the DICOM header, when combined with a Breast Tomo Series results in incorrect measurements.

Low

FDAJan 10, 2024Nationwide• FUJIFILM Healthcare Americas Corporation

Synapse PACS v7.2.200 (Fujifilm) – Measurement Error (2024)

Measurements on a Secondary Capture 2D image, that does not have pixel spacing in the DICOM header, when combined with a Breast Tomo Series results in incorrect measurements.

Low

FDAJan 10, 2024Nationwide• FUJIFILM Healthcare Americas Corporation

Synapse PACS v7.1.000 (Fujifilm) – Measurement Error (2024)

Measurements on a Secondary Capture 2D image, that does not have pixel spacing in the DICOM header, when combined with a Breast Tomo Series results in incorrect measurements.

Low

FDAJan 10, 2024Nationwide• FUJIFILM Healthcare Americas Corporation