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.

18151–18175 of 50404

  • HighNHTSA·22V063000·2022-02-04

    Tesla Model Y Boombox Feature May Obscure Pedestrian Warning System

    Tesla is recalling certain 2020-2022 Model Y vehicles because the Boombox feature can obscure the Pedestrian Warning System sounds, creating a collision risk. Tesla will disable the Boombox in Drive, Neutral, and Reverse modes via software update.

    Product
    TESLA — TESLA MODEL 3, MODEL X, MODEL Y, MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E006000·2022-02-03

    Nexxpro Recalls X.R2 Motorcycle Helmets Due to Impact Protection Defect

    Nexxpro is recalling specific X.R2 motorcycle helmets because they may not adequately protect the wearer in a crash. Owners will receive free replacements.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V058000·2022-02-03

    Altec Recalls 2017-2021 LS60 Aerial Devices Due to Bearing Bolt Risk

    Altec is recalling 2017-2021 LS60 aerial devices because bearing bolt washers may interfere with welds, causing bolts to break and increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V059000·2022-02-03

    Class C Motorhomes Recalled for Defective Steering Bolts

    Jayco is recalling certain 2021-2022 Entegra Coach Accolade and Jayco Seneca Class C motorhomes because steering arm and tie rod bolts may fracture, causing loss of steering control. Free replacement available.

    Product
    ENTEGRA — ENTEGRA, JAYCO ACCOLADE XL, SENECA PRESTIGE, SENECA, ACCOLADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22719·2022-02-03

    River Street Five-Drawer Chests Recalled for Tip-Over and Entrapment Hazards

    BFG North Carolina is recalling about 1,380 River Street Five-Drawer Chests sold at Rooms To Go from February 2019 through October 2021. The dressers are unstable if not anchored to the wall, posing tip-over and entrapment hazards that may result in death or serious injuries to children.

    Product
    River Street Five-Drawer Chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V057000·2022-02-03

    Highland Ridge RV Recalls 2022 Olympia Models Due to Electrical Grounding Defect

    Highland Ridge RV is recalling 2022 Olympia and Olympia Sport recreational vehicles because the metallic electrical box may not be grounded, posing a risk of electric shock.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT OLYMPIA, OLYMPIA SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22069·2022-02-02

    SureClose READYFIT 180° Hinge-Closer Sets Recalled for Drowning Hazard

    D&D Technologies is recalling about 1,500 SureClose READYFIT 180° hinge-closer sets because they can malfunction and fail to fully self-close gates, allowing unintended access to pools and posing injury and drowning hazards to young children.

    Product
    SureClose® READYFIT 180° Hinge-Closer Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0528-2022·2022-02-02

    MAGEC 1 System Recalled for Post-Implantation Component Fractures

    The MAGEC 1 System implantable medical device is being recalled due to documented post-implantation fractures of an internal metallic component. The recall affects approximately 3,056 units manufactured before March 26, 2015 and distributed worldwide.

    Product
    MAGEC 1 System
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0617-2022·2022-02-02

    G&C Foods Gouda Cheese Recall for Undeclared Wheat

    G&C Food Distributors & Brokers Inc. is recalling Gouda cheese that may contain undeclared wheat. The product was distributed to food service facilities in Connecticut, New Jersey, New York, Pennsylvania, and Tennessee.

    Product
    GOUDA CHEESE; INGREDIENTS: CULTURED PASTEURIZED MILK, SALT, ENZYMES, ANNATTO COLOR; Distributed By: G&C Foods; ALLERGEN: MILK; CONTAINS: 1 BAG; Product is for Food Service Only; KEEP REFRIGERATED
    Category
    Food
    Distribution
    5 states
  • HighFDA (Drugs)·D-0397-2022·2022-02-02

    Ceftazidime Sterile Ophthalmic Solution Lacks Sterility Assurance

    Edge Pharma is recalling Ceftazidime sterile ophthalmic solution for intraocular injection due to lack of assurance of sterility. The recall affects 168 syringes distributed nationwide.

    Product
    Ceftazidime, Sterile Ophthalmic Solution for Injection, Preservative Free (11.25 mg/0.5 mL (22.5 mg/mL), 0.5mL single use syringe for Intraocular Injection, Edge Pharma, LLC, 656 Hercules Dr., Colchester, VT 05446, NDC 05446-0733-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22066·2022-02-02

    Children's Robes Recalled for Flammability Standards Violation

    BAOPTEIL-branded children's robes sold on Amazon fail to meet federal flammability standards for children's sleepwear, posing a burn hazard. About 3,800 units sold from December 2019 through August 2021 are affected.

    Product
    Children's Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0405-2022·2022-02-02

    Methacholine Challenge Test Kit Recalled for Lack of Sterility Assurance

    Edge Pharma, LLC is recalling Methacholine Challenge 5-Syringe Test Kits nationwide due to lack of assurance of sterility. The sterile inhalation solution may not meet sterility standards.

    Product
    Methacholine Challenge 5-Syringe Test Kit, Sterile Inhalation Solution, Preservative Free, 3 mL per syringe,(NDC 05446-1600-05), Kit includes; individual syringe: Methacholine Chloride,16 mg/mL (contains 48 mg) NDC 05446-1241-01; Methacholine Chloride 4 mg/mL (contains 12mg)…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0517-2022·2022-02-02

    Diagnostic Imaging Angiography System Software Defects Recalled by Siemens

    Siemens is recalling 23 Artis icono angiography systems due to four software defects that could disable imaging, corrupt images, and cause unexpected shutdowns during patient procedures.

    Product
    Artis icono floor with software VE20C-diagnostic imaging angiography system Model: 11327700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0515-2022·2022-02-02

    Siemens Diagnostic Angiography System Recalled for Multiple Software Defects

    Siemens is recalling its Artis pheno diagnostic angiography system (12 units) due to four software defects that may prevent imaging, corrupt images, or cause unintended shutdowns during clinical use.

    Product
    Artis pheno with software VE20C- diagnostic imaging angiography system Model: 10849000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0516-2022·2022-02-02

    Artis icono diagnostic imaging system software defects recalled nationwide

    Siemens is recalling 72 units of Artis icono biplane diagnostic imaging systems nationwide due to four software issues that could disable x-ray capability, corrupt diagnostic images, or cause unexpected shutdowns during procedures.

    Product
    Artis icono biplane with software VE20C-diagnostic imaging angiography system Model: 11327600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0526-2022·2022-02-02

    Footrest accessory recalled for missing friction rubber block

    FDA recalls Intelli-C footrest accessories due to missing friction rubber blocks in the clamping mechanism. The defect may cause the footrest to slip during use.

    Product
    1. Footrest ( use exclusively in combination with Intelli-C devices) 2. Shoulder support ( use exclusively in combination with Intelli-C devices)
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Food)·F-0521-2022·2022-02-02

    Inglehoffer Seafood Tartar Sauce Recalled for Undeclared Soy

    Beaverton Foods Inc is recalling Inglehoffer Seafood Tartar Sauce with Lemon & Capers because the ingredient label declares soybean oil but does not adequately disclose soy as an allergen, posing a risk to consumers with soy allergies.

    Product
    Inglehoffer Seafood Tartar Sauce With Lemon & Capers, 8.25oz (234g) jar, UPC 0 71828 01114 1. The label is read in parts: "***Inglehoffer*** Seafood TARTAR SAUCE WITH LEMON & CAPERS*** INGREDIENTS: SOYBEAN OIL, WATER, CUCUMBERS, EGGS, WHITE DISTILLED VINEGAR, SALT, MUSTARD…
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·22V048000·2022-02-02

    2021-2022 Keystone RV models recalled for tire belt separation defect

    Keystone is recalling 2021-2022 Raptor and 2021 Montana RVs with certain Sailun tires that may experience belt separation. Belt separation could cause loss of vehicle control and increase crash risk.

    Product
    KEYSTONE — KEYSTONE MONTANA, RAPTOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0522-2022·2022-02-02

    GAT SPORT JETFUEL DIURETIC dietary supplement recalled for undeclared milk

    World Health Products LLC is recalling GAT SPORT JETFUEL DIURETIC capsules because they may contain undeclared milk, a common allergen. The product was distributed across most U.S. states and internationally.

    Product
    GAT SPORT JETFUEL DIURETIC; FOR RELIEF OF WATER WEIGHT GAIN; Muscle Defining Formula; Stimulant Free Natural Herbal Actives; 90 Oil-Infused Capsules; Dietary Supplement; Other Ingredients: Gelatin (Capsule), Dicalcium Phosphate, Microcrystalline Cellulose, Magnesium Stearate…
    Category
    Food
    Distribution
    39 states