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.

276–300 of 52881

  • HighFDA (Devices)·Z-2805-2026·2026-08-05

    Permobil Recalls M5 Corpus Power Wheelchairs Due to Firmware Drive Inhibit Issue

    Permobil Inc. is recalling 715 M5 Corpus Power Wheelchairs (REF 120032) because firmware versions 1.27 through 1.57 lack drive inhibit logic, which may allow driving under restricted conditions and cause instability.

    Product
    M5 Corpus Power Wheelchair REF,120032
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2795-2026·2026-08-05

    Permobil M3 Corpus Power Wheelchair Recalled Over Firmware Stability Issue

    Permobil is recalling M3 Corpus Power Wheelchairs with firmware version 1.26.2 because the firmware lacks a speed restriction when the seat lift exceeds 50 mm, which may cause falls or tip-overs.

    Product
    Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V504000·2026-08-03

    Rosenbauer Recalls Emergency Vehicles with Faulty Display Units

    Rosenbauer is recalling certain 2024-2026 emergency vehicles because a display unit may fail, preventing the activation of exterior lights and firefighting equipment.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, COMMERCIAL M2-106, COMMERCIAL HV507
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E052000·2026-08-03

    Daimler Trucks Recalls Aftermarket Grote Headlamps Due to Software Error

    Daimler Trucks North America is recalling aftermarket Grote Headlamps because a software error may cause low beams to illuminate improperly, increasing crash risk.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V503000·2026-08-03

    Forest River Recalls 2027 Freelander and Leprechaun RVs for Fire Risk

    Forest River is recalling 2027 Freelander and Leprechaun recreational vehicles because a missing breaker leaves the power feed wire without overcurrent protection, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER FREELANDER, LEPRECHAUN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V502000·2026-07-31

    Royal Truck Recalls Traffic Control Vehicles Due to Solar Panel Screw Loosening

    Alamo Group is recalling 2022-2026 Royal Truck & Equipment Class 2 Traffic Control trucks because solar panel screws may loosen, causing the panel to detach and strike others.

    Product
    ROYAL TRUCK & EQUIPMENT — ROYAL TRUCK & EQUIPMENT TRAFFIC CONTROL VEHICLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V499000·2026-07-30

    Brinkley RV Recalls 2027 Model I Trailers Due to Ladder Defect

    Brinkley RV is recalling 2027 Model I trailers because the exterior ladder may not be properly secured, posing a risk of injury if it detaches.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V501000·2026-07-30

    Autocar Recalls 2023-2027 ACTT Tractors Due to ABS ECU Securing Issue

    Autocar is recalling 2023-2027 ACTT terminal tractors because the ABS Electronic Control Unit may be improperly secured, potentially causing system failure and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR E-ACTT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26656·2026-07-30

    Baby doll playsets recalled for choking hazard under federal small parts ban

    About 1,034 Mommy's Baby Lovely Deluxe Baby Doll Playsets sold on Temu contain small parts that pose a choking hazard to children under three. No injuries reported.

    Product
    Mommy's Baby Lovely Deluxe Baby Doll Playsets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26650·2026-07-30

    Movie souvenir cups and popcorn helmets recalled for button battery ingestion hazard

    About 55,350 Fantastic Four drinking cups and Captain America popcorn helmets with LED lights have accessible button cell batteries and lack the warning labels required by Reese's Law.

    Product
    Fantastic Four Drinking Cups and Captain America Popcorn Helmet Containers with LED Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26658·2026-07-30

    Woodure toddler kitchen step stools recalled after 22 tip-over reports

    About 91,000 Woodure toddler tower stools can collapse or tip over, with openings a child's torso can pass through. Woodure reports 22 incidents and 15 injuries involving scrapes, cuts and bruises.

    Product
    Woodure Toddler Kitchen Step Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-07302026-01·2026-07-30

    Curry chicken salad flagged for possible Listeria contamination in two states

    FSIS issued a public health alert for 8-oz Curry Chicken Salad from Mary's Harvest Fresh Foods, shipped to retailers in Oregon and Washington. No illnesses have been confirmed.

    Product
    Mary's Harvest Fresh Foods, Inc. — FSIS Issues Public Health Alert for Chicken Salad Product that May Be Contaminated with Listeria
    Category
    Food
    Distribution
    2 states
  • HighCPSC·26654·2026-07-30

    Sloosh dive sticks recalled for impalement risk under federal dive stick ban

    Joyin expanded its recall of Sloosh dive sticks to models 40003 and 16154 alongside model 40041. The sticks exceed the federal compression limit and pose an impalement hazard. No injuries reported.

    Product
    Sloosh Dive Sticks, models 40041, 40003 and 16154
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26646·2026-07-30

    KAIFAM 5-drawer dressers recalled for tip-over and entrapment hazards

    About 1,980 KAIFAM 5-drawer metal dressers sold on Amazon are unstable when not anchored to a wall and violate the STURDY Act standard. No injuries reported.

    Product
    KAIFAM 5-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1179-2026·2026-07-29

    Brooklyn Roasting Company Pasteurized Cold Brew Concentrate Recalled Due to Botulism Risk

    Brooklyn Roasting Works LLC is recalling Brooklyn Roasting Company Pasteurized Cold Brew Concentrate because ambient storage may lead to Clostridium botulinum toxin formation.

    Product
    Brooklyn Roasting Company Pasteurized Cold Brew Concentrate; 2.5gal; bag in a box distributed between 04/01/2026 and 06/20/2026.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0716-2026·2026-07-29

    Rohto Cooling Eye Drops Max Strength Recalled Due to Sterility Concerns

    Rohto-Mentholatum (Vietnam) Co., Ltd. is recalling Rohto Cooling Eye Drops Max Strength because there is a lack of assurance regarding the product's sterility.

    Product
    Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0.03%, polysorbate 90, 0.2%), Sterile 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310742011012, NDC 10742-8158-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0727-2026·2026-07-29

    Naropin Injection Recall Over Particulate Matter Contamination

    Fresenius Kabi is recalling 92,600 vials of NAROPIN (ropivacaine hydrochloride) injection, 0.5%, 10/2028, due to the presence of particulate matter, including hair, found in the product.

    Product
    NAROPIN — NAROPIN (ROPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0721-2026·2026-07-29

    ROHTO DRY-AID Eye Drops Recalled Due to Sterility Concerns

    The FDA is recalling ROHTO DRY-AID cooling eye drops due to lack of assurance of sterility. The product was distributed nationwide in the United States.

    Product
    Rohto Cooling Eye Drops Dry Aid (povidone 0.68%, propylene glycol 0.3%), Sterile, TWIN PACK 0.34 FL OZ (10 mL) each, Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310742011159, NDC 10742-8162-2
    Category
    Drug
    Distribution
    Distributed nationwide