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.

526–550 of 50462

  • HighFDA (Devices)·Z-2822-2026·2026-08-05

    Bar Code Reader Wands for GEM Premier Blood Analyzers Recalled Due to Misidentification Risk

    Instrumentation Laboratory is recalling Bar Code Reader (BCR) wands used with GEM Premier 5000 and 7000 systems because they may assign patient results to the wrong patient ID.

    Product
    Brand Name: GEM Premier 7000 with iQM3 Product Name: GEM Premier 7000 with iQM3 Model/Catalog Number: 00000015279 Intelligent Quality Management 3 (iQM3) is used as the quality control (QC) and assessment system for the GEM Premier 7000. portable blood analyzer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2810-2026·2026-08-05

    Arterial Cannula Recalled Due to Risk of Pinhole Leaks During Bypass

    Medtronic is recalling 3,621 EOPA 3D Arterial Cannula DIL TIP 22FR units because pinhole leaks may occur during cardiopulmonary bypass, risking hypovolemia, vessel injury, hypotension, ischemia, and organ dysfunction.

    Product
    EOPA 3D Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 78222
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2812-2026·2026-08-05

    Medical Convenience Kits Recalled Due to Supplier Quality Issue with Lidocaine Injection

    Windstone Medical Packaging is recalling 15 AMS spinal convenience kits, lot 230451, because they contain Elevaris Lidocaine HCl injection recalled for supplier quality issues.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: SPINAL KIT, Part Number AMS13683A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2801-2026·2026-08-05

    Neurological Sponges Recalled Due to Potential Variability in Endotoxin Levels

    Medicom is recalling specific lots of Ritmed Neurological Sponges (Models 55992C to 55998C) because of potential unexpected variability in endotoxin levels.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Neuro Pack, Pack Number AMS12195C; 2) Neuro Pack, Pack Number AMS12195D; 3) Neuro Pack, Pack Number AMS12307; 4) Neuro Spine Pack, Pack Number AMS16313; 5) Lami Kukkar Pack, Pack Number AMS17958…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2800-2026·2026-08-05

    Ritmed Neurological Sponges Recalled Due to Potential Endotoxin Level Variability

    Medicom is recalling specific lots of Ritmed Neurological Sponges (Models 55992C to 55998C) because of potential unexpected variability in endotoxin levels.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Pack Number AMS12206; 2) ENT Pack, Pack Number AMS15517; 3) ENT Facial Pack, Pack Number AMS15863A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2830-2026·2026-08-05

    Stryker Hoffmann II Carbon Connecting Rods Recalled Over Potential Cracking

    Stryker GmbH is recalling Hoffmann II Carbon Connecting Rods (catalog 50796060) because they may crack after cleaning and sterilization. The recall covers all lots and about 9,658 units distributed worldwide.

    Product
    Stryker Hoffmann II Connecting Rod Micro 3 x 60mm. Catalog Number: 50796060.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2821-2026·2026-08-05

    Bar Code Reader Wands for GEM Premier Blood Analyzers Recalled Due to Misidentification Risk

    Instrumentation Laboratory is recalling Bar Code Reader (BCR) wands used with GEM Premier 5000 and 7000 systems because they may assign patient results to the wrong patient ID.

    Product
    GEM Premier 5000 with IQM2 Model/Catalog Number: 00024019255 and GEM Premier 7000 with iQM3 Model/Catalog Number: 00000015279 Portable blood analyzer system. Affected Accessory: Bar Code Reader (BCR) Wand Part No. 00024015859
    Category
    Medical Device
    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 LEPRECHAUN, FREELANDER
    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·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 HV507, COMMERCIAL M2-106
    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
  • 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·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·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
  • 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·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