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.

3676–3700 of 52939

  • HighNHTSA·25V584000·2025-09-06

    Spartan Fire Recalls Fire Trucks Due to Door Latch Defect

    Spartan Fire is recalling specific 2023-2026 fire trucks because a door latch defect may prevent the cab door from opening, potentially trapping occupants.

    Product
    SPARTAN FIRE — SPARTAN FIRE, KME METROSTAR, redundant PREDATOR, PREDATOR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V583000·2025-09-05

    Honda CRF1100 Africa Twin Motorcycles Handlebar Switch Corrosion

    Honda is recalling certain 2020–2025 CRF1100 Africa Twin motorcycles due to corrosion of the left handlebar switch harness, which may disable the horn or headlight beam-switching function. This electrical failure increases crash and injury risk.

    Product
    HONDA — HONDA CRF1100
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V582000·2025-09-05

    2025 Acura RDX Electric Power Steering Software Calibration Defect

    Honda is recalling certain 2025 Acura RDX vehicles because the electric power steering software may not be properly calibrated, which can cause loss of power steering assist and increase crash risk.

    Product
    ACURA — ACURA RDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V577000·2025-09-04

    2023–2025 Toyota BZ4X, Lexus RZ, and Subaru Solterra HVAC Defroster System Recall

    Toyota is recalling certain 2023–2025 BZ4X, Lexus RZ, and Subaru Solterra vehicles because the defroster and defogger system may become inoperative due to electrical compressor failure, decreasing driver visibility and increasing crash risk.

    Product
    LEXUS — LEXUS, TOYOTA, SUBARU RZ, BZ4X, SOLTERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V573000·2025-09-04

    2025 Chrysler Pacifica side curtain air bags recalled for inadequate pressure retention

    Chrysler is recalling certain 2025 Pacifica and Voyager vehicles due to defective side curtain air bags. The air bags may have insufficient pressure retention from improperly sealed seams, increasing the risk of ejection during a crash.

    Product
    CHRYSLER — CHRYSLER PACIFICA, VOYAGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V580000·2025-09-04

    IC Bus School Buses Recalled for Structural Reinforcement Defect

    International Motors is recalling certain 2016-2026 IC Bus CESB and 2016-2021 RESB school buses due to missing or incomplete underfloor reinforcement that may compromise crash safety. Owners should contact a dealer for free inspection and installation.

    Product
    IC BUS — IC BUS RESB, CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25458·2025-09-04

    Firearm chamber locks recalled because they can be forcibly removed

    About 300 AR-15 Chamber Lock Pro firearm locks shipped between June 2 and July 15, 2025 are recalled because a manufacturing defect allows them to be forcibly removed, permitting access to the firearm.

    Product
    AR-15 Chamber Lock Pro Firearm Locks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V578000·2025-09-04

    Jayco Recalls 2026 Seismic Fifth Wheels for Incorrect Weight Labels

    Jayco is recalling 2026 Seismic fifth wheel travel trailers because the certification label lists an incorrect Gross Axle Weight Rating (GAWR).

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E054000·2025-09-03

    Magna Recalls Rearview Cameras on Ford and Chrysler Vehicles

    Magna International is recalling rearview cameras installed on certain Ford and Chrysler vehicles because they may display a blank or inverted image, increasing crash risk.

    Product
    BACK OVER PREVENTION: SENSING SYSTEM: CAMERA recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2424-2025·2025-09-03

    Canal filling stems recalled after unidentified substance found during retrospective evaluation

    ELEOS Segmental Stem Canal Filling straight slotted splined 2/3 plasma implants are recalled because an unidentified substance of unknown impact was found on devices. 15 units are affected.

    Product
    ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS SEGMENTAL STEM CANAL FILLING STRAIGHT SLOTTED SPLINED 2/3 PLASMA. Canal filling stem implants.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2468-2025·2025-09-03

    Craniotomy and shunt packs recalled over unjustified sterilization of certain components

    American Contract Systems craniotomy and shunt procedure packs are recalled because the firm cannot confirm that product sterilization assurance requirements were met. 204 units are affected.

    Product
    AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) SFCH CRANI PACK (PS 132432), MODEL/ITEM NUMBER UICR10W; 2) SFCH SHUNT PACK (PS 139798), MODEL/ITEM NUMBER UISH55V.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Drugs)·D-0605-2025·2025-09-03

    Alcohol prep pads recalled for isopropyl alcohol below labeled concentration

    Rite Aid Pharmacy first aid alcohol prep pads are recalled nationwide because isopropyl alcohol levels fall below the labeled concentration. The recall covers 984,000 pads.

    Product
    ALCOHOL — ALCOHOL (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2341-2025·2025-09-03

    OEC 9800 C-arm systems recalled over missing collimator cover lead tape

    GE HealthCare OEC 9800 C-arm systems are recalled because impacted units are missing the full layer of lead tape in the collimator covers, slightly increasing radiation exposure.

    Product
    GE HealthCare OEC 9800.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V572000·2025-09-03

    Ford Recalls Vehicles Due to Rearview Camera Display Issues

    Ford is recalling specific 2015-2019 vehicles because the rearview camera may display a distorted, inverted, or blank image, increasing crash risk.

    Product
    FORD — FORD, LINCOLN EDGE, MUSTANG, F-550 SD, EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2462-2025·2025-09-03

    Foley catheters recalled because obstructed lumen may prevent bladder drainage

    Bardex Lubri-Sil I.C. Foley catheters and related tray systems are recalled because the catheter may have an obstructed lumen, which may prevent the bladder from draining. 175,158 units are affected.

    Product
    Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated All-Silicone Foley Catheter 5cc Balloon, REF: 119314; SureStep Foley Tray System Lubri-Sil I.C. Complete Care, REF: A319514A; Bard Silver Lubri-Sil Foley Tray Temperature Sensing with Bard Hydrogel and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0549-2025·2025-09-03

    Raw frozen shrimp recalled over possible contamination with cesium-137

    Great Value and Sea Best branded raw frozen shrimp in bulk master cartons, product of Indonesia, is recalled because the product may be contaminated with Cesium-137. 33,164 pounds are affected.

    Product
    Great Value branded and Sea Best branded raw frozen shrimp in bulk packaging, master cartons. Master carton case is 20 lbs (10 x 2lbs retail bags), and 18 lbs (12 x 1.5lbs retail bags) and (10x1lb retail bags), Product of Indonesia, Keep Frozen, Distributed by Beaver Street Fish
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2466-2025·2025-09-03

    Cystoscopy and TUR packs recalled over unconfirmed sterilization assurance requirements

    American Contract Systems cysto and TUR basin packs are recalled because the firm cannot confirm that product sterilization assurance requirements were met. 1,127 units are affected.

    Product
    AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) CYSTO, Model/Item Number ASCY24A; 2) CYSTO PACK, Model/Item Number BUCY78E; 3) CYSTO PACK, Model/Item Number LMCP22T; 4) TUR BASIN PACK, Model/Item Number LMTU31T; 5) CYSTO, Model/Item Number SA
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·H-0535-2025·2025-09-03

    Graham cracker meal recalled because label lists no ingredients or allergens

    Baker's Authority Graham Cracker Meal in 5 lb bags is recalled because the label does not list its ingredients, including the major food allergens wheat and soy. 70 units are affected.

    Product
    Baker's Authority Graham Cracker Meal; 5lb bag; stored dry at room temperature; packaged in silver bag
    Category
    Food
    Distribution
    17 states
  • HighFDA (Devices)·Z-2425-2025·2025-09-03

    Limb salvage stem extensions recalled after unidentified substance found on devices

    ELEOS Segmental Limb Salvage System straight splined slotted stem extensions are recalled because an unidentified substance of unknown impact was found on devices during a retrospective evaluation. 554 units are affected.

    Product
    ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS STEM EXTENSION, STRAIGHT, SPLINED, SLOTTED. Canal filling stem implants.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2452-2025·2025-09-03

    Surgery trays recalled because they contain recalled tourniquet cuffs

    Medline General Surgery Trays are recalled because they contain recalled Stryker Color Cuff tourniquet cuffs whose flange may detach, compromising air pressure and risking tourniquet failure. 1,145 units are affected.

    Product
    The Medline General Surgery Tray is customized to meet requirements of the hospitals and health care professionals utilizing them. The kit is provided sterile, single-use and includes a range of components dependent upon the specific procedure. These kits will be assembled using
    Category
    Medical Device
    Distribution
    Distributed nationwide