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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19926–19950 of 27461

  • HighCPSC·23721·2023-01-12

    LG 86-inch Smart Televisions Recalled for Tip-Over and Entrapment Hazards

    LG is recalling about 52,000 of its 86-inch smart televisions with stands because the stand can become unstable, creating tip-over and entrapment hazards that can result in injuries or death. Consumers should immediately detach the stands and place the TVs in a safe location away from children.

    Product
    LG 86-inch smart televisions and stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0219-2023·2023-01-11

    Three Gold Coins Dried Mushrooms Recalled Due to Salmonella Contamination

    Three Gold Coins Dried Mushrooms Sliced have been recalled due to Salmonella contamination. Affected product was distributed across 15 U.S. states.

    Product
    Three Gold Coins, Dried Mushrooms Sliced (01276) Nam Meo Soi L- 24x10.5 oz.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0216-2023·2023-01-11

    Power Life Protein Powder Recalled Due to Undeclared Milk

    Power Life High Impact Plant Protein in chocolate flavor is recalled because the product label does not declare milk as an ingredient, creating a serious allergic reaction risk for milk-allergic consumers.

    Product
    Power Life by Tony Horton High Impact Plant Protein Chocolate Flavor NET WT 446 G (15.7 OZ) Ingredients: Vegan Protein Mix (pumpkin, sunflower, flax)(as ProteoSMART), Mung Bean Protein, myHMB (Calcium Beta-hydroxy-Beta-Methlbutyrate), Alkalized Cocoa Powder, Pea Protein Powder,
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0221-2023·2023-01-11

    Dried mushrooms recalled due to Salmonella contamination

    Three Gold Coins dried mushrooms have been recalled due to Salmonella contamination. Consumers should not consume the product.

    Product
    Three Gold Coins, Dried Mushrooms (01277) Nam Meo Nguyen Tai L- 24x10.5 oz
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0214-2023·2023-01-11

    Cranberry Sweets Meltaway Recalled for Undeclared Peanut Allergen

    Cranberry Sweets & More Inc is recalling Peanut Butter Meltaway chocolates mislabeled as Mint Meltaways. The product contains undeclared peanut, a major food allergen, posing risk to allergic consumers.

    Product
    Recalled Meltaways product is packaged in clear cellophane bags, net wt. 4oz and 8 oz. and has no UPC. The front label is read Mint Meltaways, Cranberry Sweets and more, Coos Bay, OR 97402. The back label is read Heirloom Mint Meltaways, Ingredients: Milk Chocolate (***soy lecit
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0218-2023·2023-01-11

    Three Gold Coins Dried Mushrooms Recalled for Salmonella Contamination

    Three Gold Coins brand dried mushrooms have been recalled due to Salmonella contamination. Approximately 341.2 cases were distributed across 15 U.S. states.

    Product
    Three Gold Coins, Dried Mushrooms Sliced (01051) Nam Meo Soi S- 50x2.5 oz
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0224-2023·2023-01-11

    Culvers Tartar Sauce 2 oz Cups Recalled for Undeclared Allergens

    Culvers tartar sauce is being recalled because it contains undeclared fish, soy, and milk allergens. Food service locations should remove the product immediately.

    Product
    Culvers Tartar Sauce 2 oz. plastic cups
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0220-2023·2023-01-11

    Three Gold Coins Dried Mushrooms Recalled for Salmonella Contamination

    Tai Phat Wholesalers LLC is recalling Three Gold Coins Dried Mushrooms due to Salmonella contamination. The product was distributed to multiple states including Florida, New York, and Pennsylvania.

    Product
    Three Gold Coins, Dried Mushrooms (01052) Nam Meo Nguyen Tai S- 50x2.5 oz
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0796-2023·2023-01-11

    Measles Antibody Test Kits Recalled Due to Temperature Excursion

    Biomerieux Inc recalled VIDAS Measles IgG diagnostic test kits due to temperature and time excursions during storage or transport. Affected batch 1009421810 distributed nationwide; product performance cannot be guaranteed.

    Product
    VIDAS CLINICAL VIDAS MEASLES IGG 60TESTS, CATALOG 30219
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0834-2023·2023-01-11

    VITEK 2 Antimicrobial Susceptibility Test Kits Recalled for Temperature Exposure

    Biomerieux is recalling VITEK 2 AST-GN70 test kits nationwide due to temperature and time excursions that may compromise test performance and diagnostic reliability.

    Product
    VITEK 2 REAGENT AST-GN70 TEST KIT 20 CARDS, CATALOG 413401
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0868-2023·2023-01-11

    VIDAS BRAHMS Procalcitonin Test System Recalled for Storage Condition Failure

    Biomerieux is recalling 47 units of the VIDAS BRAHMS Procalcitonin test system (Batch 1009301530) after determining that temperature and time exceedances compromised product performance. Affected devices may produce unreliable diagnostic results.

    Product
    VIDAS CLINICAL VIDAS BRAHMS PROCALCITONIN 60T, CATALOG 30450-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0905-2023·2023-01-11

    Randox Protein Control Material Concentration Decreased, Affecting Quality Control

    Randox Laboratories is recalling Liquid Assayed Specific Protein Control Level 3 (catalog PS2684) because the concentration of rheumatoid factor has decreased, causing quality control systems to run outside acceptable ranges and delaying test result reporting.

    Product
    Liquid Assayed Specific Protein Control Level 3- In vitro diagnostic use, in the quality control of serum on clinical chemistry and immunoassay systems Catalog Number: PS2684
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0828-2023·2023-01-11

    ETEST Minocycline Susceptibility Test Affected by Storage Temperature Exceedance

    Biomerieux is recalling ETEST CLINICAL MINOCYCLINE MC 256 clinical diagnostic tests nationwide due to storage temperature exceedance that may affect test performance and reliability.

    Product
    ETEST CLINICAL MINOCYCLINE MC 256 US S30, CATALOG 412407
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0222-2023·2023-01-11

    Super Seed Classic Crackers Recalled for Possible Rubber Contamination

    Mary's Gone Crackers is recalling Super Seed Classic Crackers due to possible rubber piece contamination in affected lots. Consumers should stop consuming the product.

    Product
    Super Seed Classic Crackers (6 pk.) 5.5 oz. UPC: 8 97580 00016 8
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0823-2023·2023-01-11

    ETEST Clinical Erythromycin test plates recalled for storage temperature deviation

    Biomerieux Inc is recalling ETEST Clinical Erythromycin EM 256 US S30 test plates (batch 1009157090) distributed nationwide. Product performance cannot be guaranteed due to temperature and time storage conditions that exceeded specifications.

    Product
    ETEST CLINICAL ERYTHROMYCIN EM 256 US S30, CATALOG 412333
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0866-2023·2023-01-11

    Biomerieux VIDAS Progesterone Tests Recalled for Storage Condition Failure

    Biomerieux is recalling VIDAS Progesterone 60 diagnostic tests (Batch 1009375960) nationwide due to storage temperature and time conditions being exceeded, preventing guaranteed product performance.

    Product
    VIDAS CLINICAL VIDAS PROGESTERONE 60 TESTS, CATALOG 30409-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0846-2023·2023-01-11

    ETEST Antibiotic Susceptibility Test Kit Recalled for Storage Degradation

    Biomerieux Inc recalled ETEST antibiotic susceptibility test kits from batch 1009384490 due to storage conditions exceeding safe temperature and time parameters, potentially affecting test accuracy.

    Product
    ETEST CLINICAL CEFTAZIDIM/AVIBACTAM US S30, CATALOG 419046
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0829-2023·2023-01-11

    Clinical Diagnostic Device Recall: ETEST Rifampicin RI 32 Performance Degradation

    Biomerieux Inc is recalling ETEST CLINICAL RIFAMPICIN RI 32 clinical diagnostic strips because temperature and time storage parameters were exceeded, and product performance cannot be guaranteed.

    Product
    ETEST CLINICAL RIFAMPICIN RI 32 US S30, CATALOG 412449
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0827-2023·2023-01-11

    ETEST Clinical Meropenem Susceptibility Test Recalled for Storage Condition Failure

    Biomerieux is recalling 3 units of ETEST Clinical Meropenem MP 32 susceptibility test (catalog 412401) nationwide due to storage temperature and time exceedances that cannot guarantee product performance.

    Product
    ETEST CLINICAL MEROPENEM MP 32 US S30, CATALOG 412401
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0848-2023·2023-01-11

    VITEK 2 Diagnostic Test Kit Recalled for Storage Parameter Exceedance

    Biomerieux is recalling 39 units of a diagnostic test kit because storage temperature and time parameters were exceeded, which may affect test performance and reliability.

    Product
    VITEK 2 REAGENT AST-ST02 TEST KIT 20 CARDS, CATALOG 420915
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0871-2023·2023-01-11

    Medical Diagnostic Device Recalled Due to Temperature and Time Excursions

    Biomerieux Inc. is recalling PPM LOMBARD diagnostic products due to storage temperature and time conditions being exceeded during distribution, which compromises the product's guaranteed performance.

    Product
    PPM LOMBARD PRODUCTS CT&IR&DB-TSA + L & P80 10PLT, CATALOG C6045-IR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0861-2023·2023-01-11

    VITEK 2 AST-XN15 Test Kit Recalled for Temperature and Time Storage Failure

    Biomerieux Inc. recalls 58 units of the VITEK 2 AST-XN15 Test Kit after storage temperatures exceeded safe limits. Performance cannot be guaranteed. Nationwide US distribution.

    Product
    VITEK 2 REAGENT AST-XN15 TEST KIT 20 CARDS, CATALOG 423829
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0794-2023·2023-01-11

    FDA Recalls Reagent Nozzle Cleaning Solution Due to Storage Temperature Exceedance

    Biomerieux Inc is recalling a reagent nozzle cleaning solution (Catalog 29588) because storage temperature and time conditions were exceeded, preventing product performance guarantee.

    Product
    PREVI COLOR GRAM REAGENT NOZZLE CLEANING SOLUTION (NA), CATALOG 29588
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0824-2023·2023-01-11

    FDA Recalls ETEST Fluconazole Susceptibility Test due to Storage Excursion

    Biomerieux Inc. is recalling ETEST CLINICAL FLUCONAZOLE FL 256 susceptibility testing kits due to storage temperature and time excursions that prevent performance verification. Affected batch 1009172020 is distributed nationwide.

    Product
    ETEST CLINICAL FLUCONAZOLE FL 256 US S30, CATALOG 412333
    Category
    Medical Device
    Distribution
    Distributed nationwide