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 the agency’s own highest classification or reported deaths or serious injuries, 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.

Filters

Agency

Category

Minimum severity

Clear filters

17776–17800 of 39601

  • SevereFDA (Food)·F-1631-2018·2018-07-11

    Caito Foods Recalls Mixed Melon Products Due to Salmonella Risk

    Caito Foods Service, Inc. is recalling multiple brands of mixed melon products due to potential Salmonella contamination. The products were distributed in 23 states.

    Product
    Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Kroger FRUIT MEDLEY 1/10Z, 10 oz., UPC: 826766140176, Clear Generic Label Distributed by Renaissance Food Group Kroger FRUIT MEDLEY 1/24Z…
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Food)·F-1627-2018·2018-07-11

    Caito Foods Recalls Kroger Fruit Trays for Salmonella Risk

    Caito Foods Service, Inc. is recalling specific Kroger fruit trays with dip due to potential Salmonella contamination. The products were distributed in 23 states.

    Product
    Kroger FRUIT TRAY SM W/DIP 1/26.75Z, 26.75 oz., UPC: 826766145386 Clear Generic Label Distributed by Renaissance Food Group Kroger FRUIT TRAY LRG W/DIP 1/63Z, 63 oz., UPC: 826766145393 Clear Generic Label Distributed by Renaissance Food Group
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Drugs)·D-0894-2018·2018-07-11

    SCA Pharmaceuticals Recalls Morphine Sulfate Syringes Due to Sterility Concerns

    SCA Pharmaceuticals is voluntarily recalling specific lots of Morphine Sulfate 1 mg/mL syringes due to a potential for leakage that compromises sterility.

    Product
    Morphine Sulfate 1 mg/mL (preservative free; sulfite free) 2 mL fill 3 mL syringe, SCA Pharmaceuticals, LLC, Windsor, CT
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0911-2018·2018-07-11

    Fagron Recalls Neostigmine Methylsulfate Syringes Due to Labeling Error

    Fagron Compounding Services is recalling 390 prefilled syringes of Neostigmine Methylsulfate Injection Solution because some may be incorrectly labeled with the wrong strength.

    Product
    Neostigmine Methylsulfate Injection Solution, 3 mg per 3 mL, 1 mg per mL, 3 mL prefilled syringe, 5 syringes per package, Rx only, Fagron Sterile Services, ICB Laboratories, 8710 E 34th St. N., Wichita, KS 67205, NDC 71266-2003-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0910-2018·2018-07-11

    Fagron Recalls Neostigmine Methylsulfate Syringes Due to Labeling Error

    Fagron Sterile Services is recalling 840 prefilled syringes of Neostigmine Methylsulfate Injection Solution because they may be incorrectly labeled with the wrong strength.

    Product
    Neostigmine Methylsulfate Injection Solution, 5 mg per 5 mL, 1 mg per mL, 5 mL prefilled syringe, 5 syringes per package, Rx only, Fagron Sterile Services, ICB Laboratories, 8710 E 34th St. N., Wichita, KS 67205, NDC 71266-2003-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2345-2018·2018-07-11

    FHC microTargeting Drive System Recalled for Lead Damage Risk

    FHC, Inc. is recalling 2,952 microTargeting Drive Systems because over-tightening the depth stop screw can damage implanted leads, requiring replacement.

    Product
    microTargeting" Drive System, Product Number MT-DS
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Food)·F-1647-2018·2018-07-11

    Caito Foods Recalls Mixed Melon Products for Salmonella Risk

    Caito Foods Service, Inc. is recalling mixed melon products, including Whole Foods Market brand, due to potential Salmonella contamination.

    Product
    Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Whole Foods/ Amazon Melon Combo 20 oz., UPC: 826766811205, Whole Foods Market label
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Food)·F-1629-2018·2018-07-11

    Caito Foods Recalls Mixed Melon Products Due to Salmonella Risk

    Caito Foods Service, Inc. is recalling mixed melon products, including Kroger Salad Fiesta Fruit, due to potential Salmonella contamination.

    Product
    Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Kroger SALAD FIESTA FRUIT 1/18Z, 18 oz., UPC: 826766185641 Clear Generic Label Distributed by Renaissance Food Group
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Food)·F-1623-2018·2018-07-11

    Caito Foods Recalls Watermelon Products Due to Salmonella Risk

    Caito Foods Service, Inc. is recalling various watermelon products due to potential Salmonella contamination. The products were distributed across 23 states.

    Product
    WATERMELON CHUNKS 6/9.5Z, 9.5 oz., UPC: 81851301386; WATERMELON SPEAR 6/16Z, 16 oz., UPC: 81851301591; WATERMELON SPEAR 4/28Z, 28 oz.; UPC: 81851301607; WATERMELON CHUNKS 1/5LB, 80 oz., UPC: 81851302147; WATERMELON TRAY 1/5LB, 80 oz., UPC: 81851302239; WATERMELON CHUNK 4/18Z, 18…
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Drugs)·D-0898-2018·2018-07-11

    SCA Pharmaceuticals Recalls Norepinephrine Bags Due to Sterility Concerns

    SCA Pharmaceuticals is voluntarily recalling specific lots of Norepinephrine Bitartrate bags due to a potential for leakage that compromises sterility.

    Product
    Norepinephrine Bitartrate 4 mg (16 mcg/mL) in 0.9% Sodium Chloride 250 mL bag, SCA Pharmaceuticals, LLC, Windsor, CT
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2293-2018·2018-07-11

    Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation

    Howmedica Osteonics Corp. is recalling specific LFIT Anatomic CoCr Femoral Heads because of a higher than expected number of complaints regarding disassociation from the hip stem.

    Product
    LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2358-2018·2018-07-11

    FHC Depth Stop Adapter Recall Due to Lead Damage Risk

    FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring surgical replacement.

    Product
    microTargeting" STar" Drive System (Motorized) Distributed by Medtronic, Product Number FC8002
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-2355-2018·2018-07-11

    FHC Depth Stop Adapter Recalled for Potential Lead Damage

    FHC, Inc. is recalling the microTargeting Drive System Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring replacement.

    Product
    microTargeting" Drive System Distributed by Medtronic, Product Number FC1006
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-2354-2018·2018-07-11

    FHC Depth Stop Adapter Recall for Potential Lead Damage

    FHC, Inc. is recalling microTargeting Lead Adapters because over-tightening the depth stop screw can damage implanted leads, requiring replacement.

    Product
    microTargeting" Lead Adapter for STar" Drive, Product Number 70-CN-DB
    Category
    Medical Device
    Distribution
    46 states
  • SevereNHTSA·18V463000·2018-07-11

    Pierce Emergency Vehicles Recalled for Aerial Bracket Detachment Risk

    Pierce is recalling 2007-2017 emergency vehicles because an aerial device bracket may detach and fall, potentially striking a person below.

    Product
    PIERCE — PIERCE QUANTUM, IMPEL, VELOCITY, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0905-2018·2018-07-11

    SCA Pharmaceuticals Recalls Phenylephrine Bags Due to Leakage Risk

    SCA Pharmaceuticals is voluntarily recalling 196 bags of Phenylephrine HCL 80mg in 0.9% Sodium Chloride due to a potential for leakage that compromises sterility.

    Product
    Phenylephrine HCL 80mg in 0.9% Sodium Chloride 250 mL Bag (320 mcg/mL), SCA Pharmaceuticals, LLC, Windsor, CT
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0890-2018·2018-07-11

    Ingenus Recalls Irinotecan Hydrochloride Injection Due to Potency Issues

    Ingenus Pharmaceuticals is recalling specific lots of Irinotecan Hydrochloride Injection because they had high out-of-specification assay values for potency.

    Product
    IRINOTECAN HYDROCHLORIDE — IRINOTECAN HYDROCHLORIDE (IRINOTECAN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0895-2018·2018-07-11

    SCA Pharmaceuticals Recalls Fentanyl Bags Due to Sterility Concerns

    SCA Pharmaceuticals is voluntarily recalling 492 bags of Fentanyl admixture due to a potential for leakage that compromises sterility.

    Product
    Fentanyl (as citrate) 10 mcg/mL in 0.9% Sodium Chloride 250 mL bag, SCA Pharmaceuticals, LLC, Windsor, CT
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Food)·F-1625-2018·2018-07-11

    Caito Foods Recalls Honeydew and Cantaloupe for Salmonella Risk

    Caito Foods Service, Inc. is recalling honeydew and cantaloupe products due to potential Salmonella contamination. The recall covers approximately 3.16 million pounds distributed across 23 states.

    Product
    Honeydew, Clear Generic Label Distributed by Caito Foods; distributed at Gordon Food Service, Clear Generic Label Distributed by Caito Foods Distributed at Kroger with Clear Generic Label Distributed by Renaissance Food Group Distributed at SpartanNash Distribution…
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Food)·F-1628-2018·2018-07-11

    Caito Foods Recalls Multiple Brands of Mixed Melon for Salmonella Risk

    Caito Foods Service, Inc. is recalling mixed melon products sold under various brands due to potential Salmonella contamination.

    Product
    Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Caito Foods Disribution FRUIT SNACK TRAY 3/32Z, 32 oz., UPC: 81851301454 Clear Generic Label Distributed by Caito Foods Caito Foods…
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Devices)·Z-2351-2018·2018-07-11

    FHC Depth Stop Adapter Recalled for Potential Lead Damage

    FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage the implanted lead, requiring removal and replacement.

    Product
    microTargeting" STar" Drive System (Manual), Product Number 70-ZD-MA
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Drugs)·D-0903-2018·2018-07-11

    SCA Pharmaceuticals Recalls Phenylephrine HCL Bags Due to Sterility Concerns

    SCA Pharmaceuticals is voluntarily recalling 400 bags of Phenylephrine HCL 20 mg in 0.9% Sodium Chloride due to a potential for leakage that compromises sterility.

    Product
    Phenylephrine HCL 20 mg in 0.9% Sodium Chloride 250 mL Bag (160 mcg/mL), SCA Pharmaceuticals, LLC, Windsor, CT
    Category
    Drug
    Distribution
    0 states
  • SevereNHTSA·18V461000·2018-07-11

    Lamborghini Recalls 2015-2016 Aventador Models for Wheel Detachment Risk

    Lamborghini is recalling 2015-2016 Aventador SV vehicles because loose brake disc bolts may cause wheels to detach, increasing crash risk.

    Product
    LAMBORGHINI — LAMBORGHINI AVENTADOR, AVENTADOR ROADSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1642-2018·2018-07-11

    Caito Foods Recalls Mixed Melon Products for Salmonella Risk

    Caito Foods Service, Inc. is recalling multiple brands of mixed melon products due to potential Salmonella contamination. The recall affects approximately 3.16 million pounds of product distributed across 23 states.

    Product
    Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Walmart SALAD SEASONAL FRUIT 4/10Z 13 oz., UPC: 826766254262 Freshness Guaranteed label
    Category
    Food
    Distribution
    23 states
  • SevereNHTSA·18V458000·2018-07-10

    MV Agusta Recalls 2018 Motorcycles Due to Fork Axle Thread Damage

    MV Agusta is recalling 2018 Brutale 800 Dragster RC, F3 800, and F3 800 RC motorcycles because damaged fork axle threads may cause wheel clamping screw play and loss of control.

    Product
    MV AGUSTA — MV AGUSTA BRUTALE 800 DRAGSTER RC, F3 800, F3 800 RC
    Category
    Vehicle
    Distribution
    Distributed nationwide