The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

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Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

13051–13075 of 31489

  • ModerateFDA (Devices)·Z-2032-2024·2024-06-19

    Streptococcal A Rapid Test Kits Recalled for Unauthorized At-Home Distribution

    Wondfo USA recalls Areta Strep A test kits (Lot E03920802) distributed for unauthorized at-home and over-the-counter use. The recall affects 75,000 units distributed nationwide.

    Product
    Streptococcal A rapid test kits, labeled as: Easy Healthcare Corporation, Areta Strep A Swab Test and EASY at Home Medical LLC, Areta One Step Strep A Swab Test, Part Number ARST-100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2143-2024·2024-06-19

    Darby Dental Prophylaxis Paste Mislabeled with Incorrect Part Number

    Young Dental Manufacturing is recalling 534 units of Darby Prophylaxis Paste with 1.23% Fluoride Ion (Lot 248607) due to incorrect part number labeling. The product was labeled as part number 045032 instead of the correct 040032.

    Product
    Darby Prophylaxis Paste with 1.23% Fluoride Ion, Mint Coarse
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0552-2024·2024-06-19

    Asmanex Twisthaler inhalation powder recalled due to defective container

    Organon LLC is recalling Asmanex Twisthaler (mometasone furoate) inhalation powder nationwide due to defective containers. Affected lot #Y000085 expires April 25, 2025.

    Product
    Asmanex Twisthaler, mometasone furoate inhalation powder, 220 mcg per actuation, 30 Metered Doses, Rx Only, Manuf. for: Organon LLC, a subsidiary of Organon & Co. Product of Singapore. NDC 78206-0114-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2132-2024·2024-06-19

    Medical device nerve block needles incorrectly labeled as DEHP-free

    Stimuplex A nerve block needles labeled as DEHP-free contain trace amounts of DEHP in the adhesive. B Braun is recalling approximately 1.78 million units distributed in the US and Canada.

    Product
    Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1359-2024·2024-06-19

    TriyBrewed Coffee Concentrate Recalled for Missing Ingredient and Nutrition Labels

    Waco Bottling LLC is recalling TriyBrewed Coffee Concentrate 6oz bottles due to missing ingredient statement and nutrition label. Consumers cannot verify product contents or nutritional information.

    Product
    TriyBrewed Coffee Concentrate 6oz/177ml, amber glass bottle, 6pcs to case
    Category
    Food
    Distribution
    0 states
  • CriticalCPSC·24265·2024-06-13

    Magnetic Chess Games Recalled for High-Powered Magnet Ingestion Hazard

    About 2,600 magnetic chess games with 20 magnet pieces sold on Temu.com from December 2023 through February 2024 are recalled because the magnets violate federal toy magnet regulations and pose a serious ingestion hazard.

    Product
    1 Set Puzzle "Magnetic", "Magnetism", or "Magnetism Intelligence Strategy Game" Magnetic Battle Chess Games
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24262·2024-06-13

    Southern Telecom Recalls Lomi Roll-On Waxing Kits for Fire and Shock Hazards

    Southern Telecom is recalling about 19,500 Lomi Roll-On Waxing Kits because the power cord can overheat and short circuit, creating fire, burn, and electrical shock hazards. Two consumers suffered burns and one incident of property damage has been reported.

    Product
    Lomi Roll-On Waxing Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24266·2024-06-13

    Beaumont Plus ST Bicycles with Disc Brakes Recalled for Brake Failure Risk

    Retrospec is recalling about 530 Beaumont Plus ST bicycles with disc brakes because the front brake rotor and pads can become misaligned, potentially causing brake failure and crashes. No injuries have been reported.

    Product
    Beaumont Plus ST Bikes with disc brakes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24261·2024-06-13

    Black Diamond Neve Strap Crampons Recalled Due to Fall Hazard

    Black Diamond Equipment is recalling Neve Strap Crampons and Accessory Kits because screws connecting the heel cup to the crampon can loosen, causing the heel cup to detach and creating a fall hazard. The firm has received three reports of incidents but no injuries have been reported.

    Product
    Neve Strap Crampons and Accessory Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24263·2024-06-13

    Nap Queen Sleep Victoria Hybrid Mattresses Recalled for Fire Hazard

    Adven Group is recalling approximately 117,200 Nap Queen Sleep Victoria Hybrid Mattresses sold nationwide from February 2020 through October 2023 because they violate federal flammability regulations, posing a fire hazard.

    Product
    Nap Queen Sleep Victoria Hybrid Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24260·2024-06-13

    Daikin Air Conditioning and Heat Pump Units Recalled for Fire Hazard

    Daikin Comfort Technologies Manufacturing is recalling about 12,100 Amana, Daikin, and Goodman branded air conditioning and heat pump packaged units due to incorrect electrical ratings on the serial plate that could lead to improper wiring and fire risk.

    Product
    Amana, Daikin, and Goodman branded air conditioning and heat pump packaged units
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24264·2024-06-13

    Bambu Lab A1 3D Printers Recalled for Electric Shock and Fire Hazards

    Bambu Lab is recalling about 12,800 A1 3D printers sold between December 2023 and January 2024 due to damaged or bent heatbed cables that can short-circuit, spark, or burn through insulation, creating electric shock and fire risks. No injuries have been reported.

    Product
    Bambu Lab A1 3D printers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1340-2024·2024-06-12

    Grindsted Yogurt Stabilizer System Recalled for Potential Salmonella Contamination

    Danisco USA Inc. is recalling Grindsted Yogurt 7133 Stabilizer System due to potential Salmonella contamination. The affected ingredient was distributed to multiple U.S. states, Canada, and Mexico.

    Product
    Grindsted Yogurt 7133 Stabilizer System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • CriticalFDA (Food)·F-1314-2024·2024-06-12

    Grindsted Creamer 2395 food additive recalled for potential Salmonella

    Danisco USA Inc. is recalling Grindsted Creamer 2395 Stabilizer and Emulsifier System due to potential Salmonella contamination. The product was distributed across the US, Canada, and Mexico.

    Product
    Grindsted Creamer 2395 Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • CriticalFDA (Food)·F-1309-2024·2024-06-12

    Food Stabilizer and Emulsifier System Recalled for Potential Salmonella

    Danisco USA Inc. is recalling Grindsted Hi-Dress CDS 1880 Stabilizer and Emulsifier System due to potential Salmonella contamination. The product was distributed to facilities across multiple US states, Canada, and Mexico.

    Product
    Grindsted Hi-Dress CDS 1880 Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • CriticalFDA (Devices)·Z-1920-2024·2024-06-12

    Pediatric Patient Return Electrode Recalled for Reported Patient Burns

    Megadyne Medical Products is recalling its MEGA SOFT Pediatric Patient Return Electrode due to reports of patient burns during electrosurgical use. Approximately 1,270 units distributed worldwide are affected.

    Product
    MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient Return Electrode for patients weighing (0.8lb-50lb), (350g-22.7Kg), 66cm Long x 30.5cm Wide x 1.25cm. Electrosurgical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1339-2024·2024-06-12

    Food Preservative Recalled for Potential Salmonella Contamination

    Danisco USA Inc. is recalling Germantown Gard (A) Preservative due to potential Salmonella contamination. The recall affects 21,000 kg distributed across the US, Canada, and Mexico.

    Product
    Germantown Gard (A) Preservative, 25 kg / 55.12 lb bag
    Category
    Food
    Distribution
    24 states
  • CriticalFDA (Food)·F-1312-2024·2024-06-12

    Danisco Food Additive Recalled for Potential Salmonella Contamination

    Danisco USA Inc. has issued a recall of Grindsted ASC 2354 Stabilizer and Emulsifier System for potential Salmonella contamination. The product is distributed to multiple US states, Canada, and Mexico.

    Product
    Grindsted ASC 2354 Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • CriticalFDA (Food)·F-1328-2024·2024-06-12

    Danisco USA Inc. recalls GS 1134 Kreme WIP for potential Salmonella

    Danisco USA Inc. is recalling GS 1134 Kreme WIP, a food ingredient product, due to potential Salmonella contamination affecting multiple U.S. states, Canada, and Mexico.

    Product
    GS 1134 Kreme WIP, 25 kg / 55.12 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1305-2024·2024-06-12

    Danisco Germantown Stabilizer 1772-II Recalled for Salmonella

    Danisco USA Inc. is recalling Germantown Stabilizer 1772-II, a food stabilizer and emulsifier system, due to potential Salmonella contamination. The product was distributed across the U.S., Canada, and Mexico.

    Product
    Germantown Stabilizer 1772-II, Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1318-2024·2024-06-12

    Grindsted Creamer 2160 System Recalled for Salmonella Contamination

    Danisco USA Inc. is recalling Grindsted Creamer 2160 System bags due to potential Salmonella contamination. The recall affects 31,865.40 kg distributed across the US, Canada, and Mexico.

    Product
    Grindsted Creamer 2160 System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1337-2024·2024-06-12

    Grindsted Iced Coffee Stabilizer Recalled for Potential Salmonella

    Danisco USA Inc. is recalling Grindsted Iced Coffee 6752 Stabilizer System in 50 lb bags due to potential Salmonella contamination. The recall affects product distributed across the US, Canada, and Mexico.

    Product
    Grindsted Iced Coffee 6752 Stabilizer System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Devices)·Z-1880-2024·2024-06-12

    Arrow Ultra 8 Intra-Aortic Balloon Catheter Kit Recalled for Inflation Defect

    The FDA recalled 3,138 Arrow Ultra 8 intra-aortic balloon catheter kits globally due to potential balloon inflation failure and helium pathway damage that could compromise critical cardiac support.

    Product
    Arrow Ultra 8 IAB Intra-Aortic Balloon Catheter Kit, a) REF IAB-05830-U; b) REF IAB-05840-U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1317-2024·2024-06-12

    ASC 2138 Stabilizer and Emulsifier System Recalled for Salmonella

    Danisco USA Inc. recalls ASC 2138 Stabilizer and Emulsifier System due to potential Salmonella contamination. Affected product distributed across US, Canada, and Mexico.

    Product
    ASC 2138 Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1327-2024·2024-06-12

    Avicel-plus Food Stabilizer Additive Recalled for Potential Salmonella

    Danisco USA Inc. is recalling Avicel-plus GP 1615 Stabilizer System FCC due to potential Salmonella contamination. The affected bulk food additive was distributed to manufacturers across multiple U.S. states, Canada, and Mexico.

    Product
    Avicel-plus GP 1615 Stabilizer System FCC, 1000 kg / 2204.62 bulk bag
    Category
    Food
    Distribution
    24 states