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

18851–18875 of 114351

  • HighFDA (Food)·F-0688-2024·2024-01-10

    Scratch PASTA Co Marinara Sauce Recalled for Unlabeled Milk Allergen

    Scratch PASTA Co Marinara Sauce is recalled because the label does not list milk as a common allergen, despite the product containing milk in its butter ingredient.

    Product
    Scratch PASTA Co MARINARA SAUCE NET WT. 24.5 oz glass jar Ingredients: San Marzano Plum Peeled Tomatoes, Onion, Butter (Cream, Natural Flavor) UPC 8 50053 68700 6 Scratch Pasta Company 2204 Bedford Avenue, Suite E Lynchburg, Virginia 24503
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0692-2024·2024-01-10

    Frozen marinated milkfish recalled due to botulism risk from missing storage instructions

    Foremost Foods International is recalling Pamana Premium Marinated Bangus due to potential botulism risk. The frozen product in reduced oxygen packaging lacks required freezing and thawing instructions.

    Product
    Pamana Premium Marinated Bangus (Deboned Marinated Milkfish), Net Weight to be Weight at Time of Sale
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0634-2024·2024-01-10

    External Drainage System Collection Bags Recalled for Sterility Assurance Issues

    Natus Medical Incorporated is recalling 2,686 units of External Drainage System Collection Bags due to incomplete bioburden testing that prevents sterility assurance. Healthcare facilities and patients should contact the manufacturer or their healthcare provider for guidance.

    Product
    External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0624-2024·2024-01-10

    Serology ToRCH positive control specimen recalled for decreased HSV reactivity

    Randox Laboratories recalls SEROLOGY ToRCH lgM 2022 POSITIVE CONTROL (Lot 157SR) due to decreased HSV Type 1/2 reactivity when tested on the DiaSorin Liaison XL analyzer. The product was distributed in New York and West Virginia.

    Product
    SEROLOGY ToRCH lgM 2022 POSITIVE CONTROLI Intended for use with in vitro assays for determination of IgM antibodies to Cytomegalovirus (CMV), IgM antibodies to Rubella Virus, IgM antibodies to Toxoplasma gondii, IgM antibodies to Herpes Simplex Virus Type 1 and 2. Catalog…
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0213-2024·2024-01-10

    Prescription Oral Solution Eprontia Recalled for Out-of-Specification Impurity

    Azurity Pharmaceuticals recalls Eprontia (topiramate) oral solution nationwide because routine stability testing found an out-of-specification impurity. The chemical defect raised concerns about the drug's purity and patient safety.

    Product
    EPRONTIA — EPRONTIA (TOPIRAMATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0214-2024·2024-01-10

    Oxymetazoline Nasal Spray Recalled Due to Manufacturing Process Deviation

    Seaway Pharma is recalling oxymetazoline nasal spray due to manufacturing process deviations. No contamination was found in the final products.

    Product
    OXYMETAZOLINE HYDROCHLORIDE — OXYMETAZOLINE HYDROCHLORIDE (OXYMETAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0217-2024·2024-01-10

    Nasal Decongestant Recalled for Possible Manufacturing Water Contamination

    Quality Choice No Drip Nasal Decongestant is being recalled because purified water used in manufacturing may have contained microbial contamination. No contamination was detected in the final products.

    Product
    OXYMETAZOLINE HYDROCHLORIDE — OXYMETAZOLINE HYDROCHLORIDE (OXYMETAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0215-2024·2024-01-10

    OTC Cough Medicine Recalled for Potential Water Contamination Risk

    Seaway Pharma Inc. recalled Premier Value Tussin Cough DM due to possible microbial contamination in manufacturing water. No contamination was found in finished products and no illnesses have been reported.

    Product
    Premier Value Tussin Cough DM, Dextromethorphan HBr...Cough Suppressant, Guaifenesin...Expectorant, Alcohol Free, 8 FL OZ (237 mL) bottle, Distributed by: Pharmacy Value Alliance, LLC, 407 East Lancaster Avenue, Wayne PA 19087, UPC 8-40986-03789-4.
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0636-2024·2024-01-10

    Impella Connect medical device software portal disables unevaluated features

    Abiomed has disabled four features in the Impella Connect software portal because the FDA has not evaluated them for safety and effectiveness.

    Product
    Impella Connect, software portal for online device management that allows clinicians and Impella support staff to remotely view Impella data.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0625-2024·2024-01-10

    Reverse Shoulder Joint Implant System Recalled for Mislabeling

    Encore Medical is recalling 17 Reverse Shoulder System e+ surgical implants (Lot 381P1167) due to mislabeling. Affected units were distributed nationwide to multiple states.

    Product
    Reverse Shoulder System e+, REF 509-01-032, RSP Humeral Socket Insert, Sz. 32mm, Semi-Constrained, Sterile H2o2, CE 2797
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0216-2024·2024-01-10

    OTC Nasal Decongestant Recalled Due to Manufacturing Process Deviation

    Quality Choice No Drip nasal decongestant is being recalled due to a manufacturing deviation in water purification. No contamination was detected in the finished products.

    Product
    OXYMETAZOLINE HYDROCHLORIDE — OXYMETAZOLINE HYDROCHLORIDE (OXYMETAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0630-2024·2024-01-10

    KeySplint Hard Clear dental devices recalled for incorrect instructions

    Keystone Industries is recalling 336 units of KeySplint Hard Clear due to incorrect Instructions for Use packaged with the product. Affected units received KeySplint Soft instructions instead.

    Product
    KeySplint Hard Clear - Indicated for the fabrication of orthodontic and dental appliances such as mouthguards, nightguards, splints, repositioners, and retainers Item No.: 4220011
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0626-2024·2024-01-10

    Patella implant component recalled due to labeling error

    Encore Medical has voluntarily recalled a patella implant component (REF 130-03-738) due to mislabeling. The recall involves 2 units distributed nationwide.

    Product
    REF 130-03-738, All-Poly e + Patella, Domed Tri-Peg, 9x38mm, STERILE H2O2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V008000·2024-01-09

    PL Custom Recalls 2020-2024 Ambulances Due to Electrical Fire Risk

    PL Custom is recalling 2020-2024 Type 1 and Type 3 ambulances because a firmware defect may cause electrical circuits to overheat and catch fire.

    Product
    PL CUSTOM — PL CUSTOM TYPE I, TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V009000·2024-01-09

    Alexis Fire Equipment Recalls 2022-2023 Fire Trucks Due to Electrical Fire Risk

    Alexis Fire Equipment is recalling 56 fire trucks from 2022-2023 because a firmware defect may prevent electrical circuits from shutting off, increasing fire risk.

    Product
    ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V006000·2024-01-08

    E-One Recalls Fire Trucks Due to Electrical Fire Risk

    E-One is recalling 408 fire trucks because a wiring defect may cause electrical circuits to overheat and start a fire.

    Product
    E-ONE — E-ONE TYPHOON N, COMMERCIAL, CYCLONE E, CYCLONE N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V007000·2024-01-08

    Marion Body Works Recalls 2024 Spartan Fire MetroStar Vehicles for Brake Defect

    Marion Body Works is recalling 2024 Spartan Fire MetroStar vehicles because a defective inversion valve may delay parking brake engagement, increasing the risk of unintentional vehicle movement.

    Product
    MARION BODY WORKS — MARION BODY WORKS SPARTAN FIRE METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V005000·2024-01-08

    Coachmen Galleria motorhomes recalled for damaged wiring causing power steering loss

    Forest River is recalling Coachmen Galleria motorhomes (2020–2024) because battery boost wiring may become damaged, causing an electrical short circuit that results in loss of power steering, increasing crash risk.

    Product
    COACHMEN — COACHMEN GALLERIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V003000·2024-01-05

    Forest River Recalls 2020 Cherokee Travel Trailers Due to Draw Bar Defect

    Forest River is recalling 2020 Cherokee travel trailers because the draw bar locking mechanism may break, causing the trailer front to contact the road and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·002-2024·2024-01-05

    Salm Partners Recalls Turkey Kielbasa Due to Bone Fragments

    Salm Partners, LLC is recalling ready-to-eat turkey kielbasa products due to possible contamination with bone fragments.

    Product
    Salm Partners, LLC — Salm Partners, LLC Recalls Ready-to-Eat Turkey Kielbasa Products Due to Possible Extraneous Material Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V004000·2024-01-05

    Mickey Truck Bodies Recalls 37 Vehicles Due to Electrical Arcing Risk

    Mickey Truck Bodies is recalling 37 commercial trucks from 2020-2023 because exposed wiring on the refrigeration unit may cause electrical arcing and increase fire risk.

    Product
    MICKEY TRUCK BODIES — MICKEY TRUCK BODIES ISUZU NQR, CHEVROLET 5500 HD, HINO L6, CHEVROLET LCF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-01042024-01·2024-01-05

    Frozen Mushroom Risotto Bites Recalled For Undeclared Sesame Allergen

    USDA FSIS issued a public health alert for Wild Fork Porcini Mushroom Risotto Bites that may contain undeclared sesame. Consumers with sesame allergies should not consume these products.

    Product
    FSIS Issues Public Health Alert For Frozen Mushroom Risotto Products Due To Misbranding And Undeclared Allergen
    Category
    Food
    Distribution
    11 states
  • SevereNHTSA·24V002000·2024-01-04

    Terex Advance Concrete Mixer Trucks Recalled for Drum Separation Risk

    Terex Advance is recalling 2023-2024 concrete mixer trucks because bolts may loosen, causing the drum to separate from the vehicle.

    Product
    TEREX ADVANCE — TEREX ADVANCE CHARGER, COMMANDER, MM300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24075·2024-01-04

    Ride Aventon Sinch.2 Folding E-Bicycles Recalled for Unexpected Acceleration

    Ride Aventon is recalling about 2,300 Class 2 Sinch.2 folding e-bicycles because they can accelerate unexpectedly, causing loss of control and crash hazards. The firm has received six reports of unexpected acceleration but no injuries.

    Product
    Class 2 Sinch.2 Folding E-Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide