The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

1326–1350 of 52929

  • HighFDA (Devices)·Z-1811-2026·2026-04-22

    Arjo Tenor patient lift actuators may lose the ability to hold load

    Arjo Tenor mobile passive patient lifts are being recalled because an internal actuator component in one production batch may not meet the required mechanical strength.

    Product
    Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1824-2026·2026-04-22

    Centurion circumcision kits distributed without the required sterilization process

    Medline is recalling one lot of Centurion Circumcision Kits that was distributed without undergoing the required sterilization process and is therefore not sterile. 640 kits are affected.

    Product
    CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1821-2026·2026-04-22

    Elegance anterior cervical plates recalled over burrs on finished product

    Elegance Anterior Cervical Plates are being recalled over a quality issue involving the presence of burrs on the finished plate. The action covers 511 units.

    Product
    Brand Name: Elegance¿ Anterior Cervical Plate Product Name: ELEGANCE 1 LEVEL CERVICAL PLATE, ELEGANCE 2 LEVEL CERVICAL PLATE, ELEGANCE 3 LEVEL CERVICAL PLATE, ELEGANCE 4 LEVEL CERVICAL PLATE Model/Catalog Number: See Excel sheet attached named "FDA 5072 Product Information" So
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1822-2026·2026-04-22

    Cellex photopheresis kit centrifuge bowls may dislodge and break

    Cellex Photopheresis Kits are being recalled because the centrifuge bowl is harder to install and, if fitted improperly, may dislodge and break during priming or treatment.

    Product
    Brand Name: Cellex Photopheresis System Product Name: CELLEX Photopheresis Kit Model/Catalog Number: CLXUSA Software Version: Not Applicable Product Description: THERAKOS Photopheresis or extracorporeal photopheresis (ECP) is a photoimmune therapy where leukocytes are separa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0452-2026·2026-04-22

    FarmHouse Fresh benzoyl peroxide night lotion recalled over benzene contamination

    FarmHouse Fresh Midnight Clearing Night Lotion, a 2.5% benzoyl peroxide acne treatment, is being recalled because of chemical contamination from the presence of benzene.

    Product
    FHF Farmhouse Fresh, Midnight Clearing, NIGHT LOTION, 2.5% BENZOYL PEROXIDE ACNE TREATMENT, OTC a) 0.5 fl. oz./15ml; and b)1 fl. oz./30ml tubes; Made in the USA for FarmHouse Fresh, 8797 CR 858 McKinney, Texas
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0530-2026·2026-04-22

    Bupivacaine spinal ampules recalled nationwide over lack of sterility assurance

    Bupivacaine Hydrochloride 0.75% in 8.25% Dextrose Injection, USP ampules are being recalled for lack of assurance of sterility. The action covers 3,260,170 ampules.

    Product
    BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0529-2026·2026-04-22

    Huons lidocaine injection recalled nationwide over lack of sterility assurance

    Lidocaine HCl Injection, USP 1% in 5 mL single dose vials manufactured by Huons is being recalled for lack of assurance of sterility. All lots within expiry are affected.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V251000·2026-04-20

    Thomas Built Buses Recalls SAF-T-LINER HDX2 for Seat Belt Anchor Defect

    Daimler Trucks North America is recalling 2026-2027 Thomas Built SAF-T-LINER HDX2 buses because the driver seat belt anchor may have inadequate hardware, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E022000·2026-04-20

    Q'Straint Recalls QRT-3 Wheelchair Retractors Due to Locking Failure

    Q'Straint is recalling QRT-3 wheelchair retractors that may fail to lock, preventing proper wheelchair securement and increasing injury risk during transit.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY:WHEELCHAIR RESTRAINTS/SECUREMENT:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V254000·2026-04-20

    2026 Hyundai Tucson Hybrid and other models air bag sensor defect

    Hyundai is recalling certain 2025 and 2026 models including Tucson Hybrid, Tucson, Elantra, and Elantra N due to misassembled B-pillar impact sensors that may delay air bag deployment in a crash.

    Product
    HYUNDAI — HYUNDAI ELANTRA, ELANTRA N, TUCSON, TUCSON HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V253000·2026-04-20

    Hexagon Purus Recalls Tern RC8 Vehicles Due to Brake Display Error

    Hexagon Purus is recalling 2025-2026 Tern RC8 vehicles because a software error may cause the digital display to show incorrect air brake pressure, potentially failing to alert drivers to actual brake issues.

    Product
    HEXAGON PURUS — HEXAGON PURUS TERN RC8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V250000·2026-04-20

    Thomas Built Buses Recalls 2026-2027 SAF-T-LINER HDX2 School Buses

    Daimler Trucks North America is recalling 2026-2027 Thomas Built SAF-T-LINER HDX2 school buses because the driver seat belt anchor may have inadequate hardware.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V245000·2026-04-17

    Blue Bird Recalls 2026 All American Transit Buses for Wiper Fastener Issue

    Blue Bird is recalling 2026 All American transit buses because improperly tightened wiper fasteners may cause wipers to fail, reducing visibility and increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V246000·2026-04-17

    Blue Bird Recalls 2026-2027 All American School Buses for Wiper Fastener Issue

    Blue Bird is recalling 2026-2027 All American school buses because improperly tightened wiper fasteners may cause wipers to fail, reducing visibility and increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, ALL AMERICAN SCHOOL BUS (ELECTRIC)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V244000·2026-04-16

    2026 Ram 2500 Recall for Electronic Stability Control Defect

    Chrysler is recalling 2026 Ram 2500 trucks because steering column modules may cause a loss of electronic stability control, increasing crash risk.

    Product
    RAM — RAM 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26424·2026-04-16

    LED finger beam lights let children access button cell batteries

    LED Finger Beam Lights are recalled because they contain button cell batteries that can be easily accessed by children, violating the mandatory safety standard for toys.

    Product
    LED Finger Beam Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26421·2026-04-16

    Fengrong Tool electric pressure washers lack a ground-fault circuit interrupter

    Fengrong Tool electric pressure washers are recalled because they lack an integral ground-fault circuit interrupter, posing shock and electrocution hazards. About 500 units are affected.

    Product
    Fengrong Tool Electric Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26420·2026-04-16

    Agiiman electric pressure washers lack a ground-fault circuit interrupter

    Agiiman pressure washers are recalled because they lack an integral ground-fault circuit interrupter, posing shock and electrocution hazards. 80 units are affected.

    Product
    Agiiman Electric Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26411·2026-04-16

    ATOYUS children's activity cubes violate the small parts ban

    ATOYUS wooden activity cubes are recalled because the xylophone screws and clock hands can detach, violating the small parts ban for toys intended for children under three.

    Product
    ATOYUS Children's Activity Cubes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26406·2026-04-16

    BATOYAK USA electric pressure washers lack a ground-fault circuit interrupter

    BATOYAK USA electric pressure washers are recalled because they lack an integral ground-fault circuit interrupter, posing shock and electrocution hazards. 360 units are affected.

    Product
    BAYOTAK USA Electric Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26407·2026-04-16

    Generac portable generators can leak fuel from the carburetor when filled

    Certain Generac portable generators are recalled because fuel can leak from the carburetor when the generator is first filled with gasoline. 114 fuel leak reports have been received; no injuries.

    Product
    Generac Portable Generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26422·2026-04-16

    Le Hao Tool pressure washers lack a ground-fault circuit interrupter

    Le Hao Tool electric pressure washers are recalled because they lack an integral ground-fault circuit interrupter, posing shock and electrocution hazards. 3,100 units are affected.

    Product
    Le Hao Tool Electric Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26419·2026-04-16

    Fisher & Paykel gas ranges can experience delayed oven ignition

    Fisher & Paykel gas ranges are recalled because the oven can experience delayed ignition, causing gas to accumulate and the oven door to open from combustion. One minor burn injury has been reported.

    Product
    Fisher & Paykel Gas Ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide