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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8601–8625 of 31218

  • HighFDA (Food)·F-0574-2025·2025-03-05

    Beverage Base Lemonade Recalled for Undeclared Yellow #5

    OCBW INC is recalling Beverage Base Lemonade products due to undeclared Yellow #5. A total of 8,847 units were distributed across eight states. Consumers with sensitivities to food dyes should not consume the product.

    Product
    Beverage Base Lemonade, 3 gallon, BIB: Best By 12/12/2025; Beverage Base Lemonade, 5 gallon, BIB: Best By 01/12/2026
    Category
    Food
    Distribution
    0 states
  • HighFDA (Drugs)·D-0248-2025·2025-03-05

    Avastin intravitreal injection syringes recalled for sterility assurance failure

    Turbare Manufacturing recalls 1,147 syringes of Avastin 1.25 mg intravitreal injection nationwide due to a quality control process deviation affecting sterility assurance.

    Product
    Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe, For Intravitreal Injection Only, Office Use Only - Not for Resale - Single Use, This drug product was repackaged by Turbare Manufacturing, 925 Jeanette Drive, Conway, AR 72032, NDC: 83556-0101-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1214-2025·2025-03-05

    Orthopedic Surgical Plates Recalled Due to Intra-Operative Locking Screw Malfunction

    Tyber Medical is recalling A.L.P.S. mvX Anatomic Lateral Fibula Plates nationwide due to reports that locking screws may pass through the locking hole during surgery, causing surgical delays.

    Product
    A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H RT: Anatomic Lateral Fibula Plate, 8-hole, Right Indicated for use in Fixation of fractures of the distal tibia Model/Catalog Number: 77070802
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1217-2025·2025-03-05

    Orthopedic Plate Locking Screw May Pass Through Hole During Surgery

    Tyber Medical is recalling A.L.P.S. mvX-P Anatomic Lateral Fibula Plates because the locking screw may pass through the locking hole during surgery, causing surgical delays.

    Product
    A.L.P.S. mvX-P: ANATOMIC LAT FIB PLATE 12H LT- Anatomic Lateral Fibula Plate, 12-Hole, Left. Inended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708121
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1207-2025·2025-03-05

    Automated Medication Cabinet Recalled Due to Fingerprint Scanner Overheating Risk

    CareFusion's BD Pyxis MedFlex automated medication cabinet is being recalled due to fingerprint scanner failure and overheating, posing a potential fire hazard in clinical settings.

    Product
    BD Pyxis MedFlex 2.0 REF 1139-00 Bio-ID Spare Parts REF 353200-01 The BD Pyxis" MedFlex is an Automated Dispensing Cabinet (ADC) intended to securely store and dispense medications and supplies to a qualified and authorized user in a clinical setting.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1215-2025·2025-03-05

    Anatomic Lateral Fibula Plate locking screw malfunction during surgery

    Tyber Medical is recalling 220 A.L.P.S. mvX Anatomic Lateral Fibula Plates due to complaints that the locking screw passes through the locking hole during surgery, causing surgical delays.

    Product
    A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Anatomic Lateral Fibula Plate, 10-Hole, Left. Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770708101
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1230-2025·2025-03-05

    BD Pyxis MedBank medication cabinets recalled for operating room contraindication labeling

    CareFusion is recalling BD Pyxis MedBank medication management cabinets due to inadequate labeling. A contraindication statement must be added to warn against use in procedure and operating rooms.

    Product
    139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK MINI 1FH-2HH MEDPASS 169-152 BD PYXIS MEDBANK MINI 2HH-1FM MEDPASS 169-150 BD PYXIS MEDBANK MINI 4HH MEDPASS 169-140 BD PYXIS MEDBANK TWR MN 3FH-8HH MEDPASS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1227-2025·2025-03-05

    BD PYXIS MEDBANK systems operating room contraindication labeling update

    BD PYXIS MEDBANK medication management systems are subject to a labeling update adding a contraindication against use in procedure and operating rooms. Approximately 6,075 units were distributed nationwide.

    Product
    138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 138911-01 BD PYXIS MEDBANK MINI CR-4HH-P 169-115 BD PYXIS MEDBANK MINI CR-4HH-P 139001-01 BD PYXIS MEDBANK MN 200 CR-2HH-1FH-P 139002-01 BD PYXIS MEDBANK MN 200 CR-2HH-1FM-P 139000-01 BD PYXIS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1228-2025·2025-03-05

    BD PYXIS MEDBANK Medication Systems: Labeling Update for Operating Room Restriction

    CareFusion is updating labeling for BD PYXIS MEDBANK medication systems to include a contraindication against use in procedure and operating rooms. Healthcare facilities should review updated labeling and ensure appropriate device placement.

    Product
    155288-01 BD PYXIS MEDBANK MINI 1FH-1FM 169-137 BD PYXIS MEDBANK MINI 1FH-1FM 155311-01 BD PYXIS MEDBANK MINI 1FH-2HH 138921-01 BD PYXIS MEDBANK MINI 1HH-1FH-1HM 155159-01 BD PYXIS MEDBANK MINI 1HH-1FH-1HM 169-101 BD PYXIS MEDBANK MINI 1HH-1FH-1HM 139122-01 BD PYXIS MEDBANK MINI
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1229-2025·2025-03-05

    BD PYXIS medication cabinets labeling update: operating room contraindication

    CareFusion is updating labeling for BD PYXIS medication management cabinets to add a contraindication statement prohibiting use in procedure and operating rooms.

    Product
    139054-01 BD PYXIS MEDFLEX MN 1000 10HH-1FM 139055-01 BD PYXIS MEDFLEX MN 1000 12HH 139053-01 BD PYXIS MEDFLEX MN 1000 2HH-2FH-3FM 139041-01 BD PYXIS MEDFLEX MN 1000 2HH-2FM 139046-01 BD PYXIS MEDFLEX MN 1000 2HH-5FM 139038-01 BD PYXIS MEDFLEX MN 1000 3FM 139040-01 BD PYXIS MEDFL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1248-2025·2025-03-05

    Medical device recall: sterilization validator with incorrect incubation time

    TERRAGENE S.A. is recalling 914 ASP BIOTRACE Auto Read 60 sterilization process challenge devices due to incorrect incubation time listed in the product instructions. The IFU lists 20 minutes instead of the correct 60 minutes.

    Product
    ASP BIOTRACE Auto Read 60 Steam BI Process Challenge Device, REF 73135.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V303000·2025-03-04

    2022-2023 Jeep Wrangler Plug-In Hybrid Battery Fuse Fastener Defect

    Chrysler is recalling certain 2022-2023 Jeep Wrangler PHEVs due to incorrect fasteners in the high voltage battery pack that can cause excessive heat and potential loss of drive power, increasing crash risk.

    Product
    JEEP — 2022 JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V184000·2025-03-04

    Nova Bus LFS Transit Buses Recalled for Battery Fire Risk

    Nova Bus is recalling 2022-2023 LFS transit buses because high voltage battery hardware may come loose and cause a short circuit, creating a fire risk.

    Product
    NOVA BUS — 2022 NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V301000·2025-03-04

    2020 RAM ProMaster Transmission Park Pawl Defect Risks Vehicle Rollaway

    RAM is recalling certain 2019-2021 ProMaster vehicles due to debris in the transmission that can prevent the park pawl from fully engaging. This may result in vehicle rollaway, increasing crash and injury risk.

    Product
    RAM — 2020 RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V205000·2025-03-03

    2024 Genesis GV70 Transmission Recall Due to Water Intrusion Risk

    Certain 2024 Genesis GV70 vehicles are recalled because water may leak into the transmission control harness, causing electrical shorts that shift the transmission from Park to Neutral, risking vehicle rollaway.

    Product
    GENESIS — 2024 GENESIS GV70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V202000·2025-03-03

    Dynamax Isata Motorhomes Recalled for Loose 12V Disconnect Fire Risk

    Dynamax Isata motorhomes (2023-2024) are recalled for a loose 12V disconnect nut that may cause electrical arcing and fire risk. Dealers will replace the part free of charge.

    Product
    DYNAMAX — 2024 DYNAMAX ISATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V204000·2025-03-03

    Hyundai and Genesis electric vehicles recalled for 12-volt battery charging failure

    Hyundai is recalling certain 2023 Ioniq 6 and related Genesis models because the 12-volt battery charger may fail, causing potential loss of drive power and increased crash risk. Repairs will be completed free of charge.

    Product
    HYUNDAI — 2023 HYUNDAI IONIQ 6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V112000·2025-03-02

    Chrysler 300 and Dodge vehicles recalled for parking brake defect

    Certain 2023 Chrysler 300, Dodge Charger, and Dodge Challenger vehicles may have improperly adjusted parking brakes that could cause vehicle rollaway. Dealers will adjust the brakes free of charge.

    Product
    CHRYSLER — 2023 CHRYSLER 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V129000·2025-03-02

    Royal Enfield Himalayan motorcycles recalled for brake caliper corrosion

    Royal Enfield is recalling 2017-2021 Himalayan motorcycles because road salt may corrode brake calipers, potentially causing brake failure and increasing crash risk.

    Product
    ROYAL ENFIELD — 2021 ROYAL ENFIELD HIMALAYAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V114000·2025-03-02

    2023-2024 Honda Odyssey and 2024 Acura RDX steering defect

    Honda is recalling certain 2023-2024 Odyssey and 2024 Acura RDX vehicles due to improper steering gear box assembly tightening. Water can enter the assembly, causing corrosion and loss of steering control.

    Product
    HONDA — 2023 HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V113000·2025-03-02

    Honda Motorcycles Recalled for Fuel Pump Failure Risk

    Honda is recalling 29,301 motorcycles with defective fuel pump impellers that may fail and cause engine stalls while driving. Affected models include the CBR600RR, CBR1000RR, and GL1800.

    Product
    HONDA — 2018 HONDA CBR600RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V111000·2025-03-02

    Jeep Wrangler Defrosting System Software Error May Impair Visibility

    Chrysler is recalling affected Jeep Wrangler and Grand Cherokee models due to a software defect in the windshield defroster system that may reduce visibility. Affected owners should contact Chrysler for a free software update.

    Product
    JEEP — 2023 JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V017000·2025-03-01

    Peterbilt and Kenworth trucks recalled for detachable mirror glass

    PACCAR is recalling certain 2022-2024 Peterbilt and Kenworth trucks because the glass lock ring on the cab mirror assembly may not be fully seated, allowing the mirror glass to detach and reduce driver visibility.

    Product
    PETERBILT — 2022 PETERBILT 548
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V033000·2025-03-01

    Porsche Panamera coolant pump electrical short circuit increases fire risk

    Porsche is recalling certain 2017-2021 Panamera models because humidity can enter the external coolant pump, causing an electrical short circuit that increases the risk of vehicle fire. Dealers will replace the pump and inspect connections at no cost.

    Product
    PORSCHE — 2019 PORSCHE PANAMERA
    Category
    Vehicle
    Distribution
    Distributed nationwide