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.

3876–3900 of 52939

  • HighFDA (Devices)·Z-2275-2025·2025-08-13

    Size 2 Guedel airways may carry small burrs that could detach

    One-piece Guedel airways, size 2, are being recalled because of potential contamination with small burrs which, if they detach, could be inhaled. 2,800 pieces are affected.

    Product
    One-piece Guedel airway, size 2, ISO 8.0, green. Model Number: 1112080.
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Drugs)·D-0563-2025·2025-08-13

    Compounded semaglutide 1.5 mg vials recalled over lack of processing controls

    Semaglutide + Cyanocobalamin 1.5 mg + 0.25 mg/0.5 mL injection solution compounded by Aequita Pharmacy is being recalled for lack of processing controls. 190 vials are affected.

    Product
    Semaglutide +Cyanocobalamin 1.5 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034.
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0562-2025·2025-08-13

    Compounded semaglutide and cyanocobalamin vials recalled over lack of processing controls

    Semaglutide + Cyanocobalamin 0.88 mg + 0.25 mg/0.5 mL injection solution compounded by Aequita Pharmacy is being recalled for lack of processing controls. 194 vials are affected.

    Product
    Semaglutide + Cyanocobalamin 0.88 mg + 0.25mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034.
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0555-2025·2025-08-13

    Compounded tirzepatide 4.4 mg vials recalled over lack of processing controls

    Tirzepatide + Niacinamide 4.4 mg + 1.0 mg/0.5 mL injection solution compounded by Aequita Pharmacy is being recalled for lack of processing controls. 170 vials are affected.

    Product
    Tirzepatide + Niacinamide 4.4 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034.
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Food)·H-0456-2025·2025-08-13

    Frederik's by Meijer sea salt flatbread crackers contain undeclared sesame

    Frederik's by Meijer Artisan Baked Sea Salt flatbread crackers, 5.5 oz, are being recalled because of undeclared sesame. 1,790 retail units are affected.

    Product
    Frederik's by Meijer Artisan Baked Sea Salt flatbread crackers net wt 5.5oz. UPC 7 13733 00048 2
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-0556-2025·2025-08-13

    Compounded tirzepatide 6.6 mg vials recalled over lack of processing controls

    Tirzepatide + Niacinamide 6.6 mg + 1.0 mg/0.5 mL injection solution compounded by Aequita Pharmacy is being recalled for lack of processing controls. 160 vials are affected.

    Product
    Tirzepatide + Niacinamide 6.6 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial, Refrigerate, Do not freeze, Aequita Pharmacy LLC, Kirkland, WA 98034.
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Food)·H-0389-2025·2025-08-13

    Breaded jalapeno mac and cheese bites used a recalled Listeria ingredient

    Breaded Jalapeno Mac & Cheese Bites in 30 lb cases are being recalled because a supplier recalled an ingredient used in the finished product for possible Listeria monocytogenes contamination. 819 cases affected.

    Product
    BREADED JALAPENO MAC & CHEESE BITES Mac & Cheese Bites, Net Wt. 30 LB. 90935, (01)10077886909359, Prepared and Packaged by LOUISA FOOD PRODUCTS, INC. St. Louis, MO 63136; COOKING DIRECTIONS: Deep fry at 350F for 3 1/2 to 4 minutes or until internal temperature reaches 160F.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-2264-2025·2025-08-13

    UIBC assay does not meet its labeled hemoglobin interference claim

    The Unsaturated Iron Binding Capacity assay is being recalled because it is not meeting the labeled hemoglobin interference claims stated in its instructions for use. 56,696 units affected.

    Product
    UIBC (Unsaturated Iron Binding Capacity), REF: OSR61205,
    Category
    Medical Device
    Distribution
    9 states
  • HighNHTSA·25V524000·2025-08-12

    Heil Recalls 2021-2022 Front End Loader Garbage Trucks Due to Weld Defect

    The Heil Co. is recalling 2021-2022 front end loader garbage trucks because missing vertical welds on the automatic front loader arm may cause it to crack and fall, increasing injury risk.

    Product
    HEIL — HEIL FRONT END LOADER GARBAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V523000·2025-08-12

    Heil Recalls 2024 Front End Loader Garbage Trucks for Fuel Solenoid Defect

    The Heil Co. is recalling 2024 front end loader garbage trucks because a fuel shutoff solenoid may fail, causing the engine to stall while driving and increasing crash risk.

    Product
    HEIL — HEIL FRONT END LOADER GARBAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V517000·2025-08-08

    Ford Recalls 2022 F-150s for Flickering Parking Lights

    Ford is recalling 2022 F-150 vehicles previously repaired under recall 22V686 because the parking lights may flicker when headlights are activated.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V510000·2025-08-08

    Lincoln Corsair rearview cameras can take in water at the connectors

    Ford is recalling certain 2020-2022 Lincoln Corsair vehicles because water may enter the rearview camera connectors, causing the image not to appear or to display distorted. 41,875 vehicles affected.

    Product
    LINCOLN — LINCOLN CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V518000·2025-08-08

    Lincoln Nautilus power windows may not reverse correctly after obstruction

    Ford is recalling certain 2024-2025 Lincoln Nautilus vehicles repaired incorrectly under a previous recall because the window automatic reversal system may not react correctly to an obstruction. 482 vehicles affected.

    Product
    LINCOLN — LINCOLN NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V516000·2025-08-08

    One Ford Mustang instrument cluster may fail to illuminate at startup

    Ford is recalling one 2024 Mustang that was repaired incorrectly under a previous recall because the Instrument Panel Cluster may not illuminate at startup or while driving.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V515000·2025-08-08

    Ford Recalls 2022 F-150s for Flickering Parking Lights

    Ford is recalling 2,361 2022 F-150 vehicles because incorrectly repaired parking lights may flicker, reducing visibility and increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V511000·2025-08-08

    Mercedes-Benz Recalls 2024 GLA Models for Headlight Aim Markings

    Mercedes-Benz is recalling 2024 GLA 250 and AMG GLA 35 4MATIC vehicles because missing headlight aim markings may cause improper aiming, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLA 35 4MATIC, GLA 250 4MATIC, GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V519000·2025-08-08

    Ford and Lincoln LED driver modules may contain a burnt diode

    Ford is recalling certain 2025 Lincoln Nautilus, Mustang Mach E and Mustang vehicles because LED Driver Modules may contain a burnt diode, causing headlights and other exterior lights to fail. 3,270 vehicles affected.

    Product
    FORD — FORD, LINCOLN MUSTANG, MUSTANG MACH E, NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V509000·2025-08-08

    Altec Recalls 2025 AP Series Vehicles Due to Brake Line Defect

    Altec is recalling 2025 AP Series vehicles because brake air line fittings may not be tightened correctly, potentially causing the emergency brakes to engage unexpectedly.

    Product
    ALTEC — ALTEC AP SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V507000·2025-08-07

    Mitsubishi Outlander PHEV liftgate gas spring cylinders corrode unexpectedly

    Mitsubishi is recalling certain 2018–2022 Outlander PHEV and 2014–2020 Outlander vehicles because liftgate gas spring cylinders may corrode, lose pressure, rupture, or cause the liftgate to fall unexpectedly, creating injury risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25424·2025-08-07

    Monica Vinader gold mini heart jewelry can contain excess cadmium

    Monica Vinader 14k Yellow Gold Mini Heart bracelets, necklaces and stud earrings are being recalled because the jewelry can contain excess levels of cadmium. About 300 units are affected.

    Product
    Monica Vinader 14k Yellow Gold Mini Heart Jewelry
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25427·2025-08-07

    La Ligne Enfant children's pajamas fail the sleepwear flammability standard

    La Ligne Enfant Bonne Nuit children's cotton pajama sets are being recalled because they violate mandatory standards for children's sleepwear flammability. About 1,185 units are affected.

    Product
    La Ligne Enfant Bonne Nuit Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25426·2025-08-07

    Séfralls minoxidil hair serum lacks the required child-resistant packaging

    Séfralls Hair Generation Serum is being recalled because it contains minoxidil, which must be in child-resistant packaging under the Poison Prevention Packaging Act. About 21,300 units affected.

    Product
    Séfralls Minoxidil Hair Generation Serum
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V505000·2025-08-07

    Suzuki Recalls Motorcycles for Excessively Bright Headlights

    Suzuki is recalling 2020-2025 DL1050 and 2020/2024 GSX-S1000S motorcycles because the upper headlight beam may be too bright, potentially blinding oncoming drivers.

    Product
    SUZUKI — SUZUKI GSX-S1000S, DL1050
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25425·2025-08-07

    LeymanKids children's pajama sets fail the sleepwear flammability standard

    LeymanKids children's two-piece pajama sets are being recalled because they violate the mandatory flammability standards for children's sleepwear. About 600 units are affected.

    Product
    LeymanKids Children's Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide