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.

17526–17550 of 50403

  • HighNHTSA·22V261000·2022-04-15

    2021 Mercedes-Benz AMG GLC63 S Headlight Failure Recall

    Mercedes-Benz is recalling certain 2021 GLC models because the headlight electrical connection may not be watertight, risking headlight failure. Reduced visibility increases crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLC63 S, AMG GLC63, AMG GLC43, GLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22115·2022-04-14

    Shell Diving Inflation Valves Recalled Due to Hypothermia Risk

    SI Tech is recalling approximately 1,670 Shell Diving Inflation Valves with International Nipples used in diving dry suits. The internal valve part can malfunction during use, causing loss of inflation and thermal protection, which poses a risk of hypothermia.

    Product
    Shell Diving Inflation Valves with Int'l Nipples for diving dry suits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V248000·2022-04-14

    2022 Jeep Compass recalled for improperly welded seat head restraints

    Chrysler is recalling 114 2022 Jeep Compass vehicles because the front seat head restraints were not properly welded, creating an increased risk of injury during a crash. Dealers will replace both head restraints at no cost.

    Product
    JEEP — JEEP COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V247000·2022-04-14

    2022 Lincoln Aviator Head Restraint Cushions May Detach

    The front-row driver and passenger head restraint cushions in certain 2022 Lincoln Aviators may detach from their assemblies when adjusted fully forward, increasing crash injury risk.

    Product
    LINCOLN — LINCOLN AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V253000·2022-04-14

    Ford Recalls 2022 F-150 Trucks for Steering Column Wiring Defect

    Ford is recalling 2022 F-150 vehicles because short steering column wiring may separate, potentially preventing the column from moving correctly in a crash.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22120·2022-04-14

    Dollar Tree Recalls 1 Million Crafter's Square Hot Glue Guns for Fire and Burn Hazards

    Dollar Tree is recalling about 1,025,000 Crafter's Square hot glue guns sold nationwide that can malfunction when plugged in, posing fire and burn hazards. Seven electrical malfunctions have been reported, including four fires and one skin irritation.

    Product
    Crafter's Square Glue Guns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V249000·2022-04-14

    2022 Jeep Grand Cherokee Recall for Turn Signal Software Error

    Chrysler is recalling 2022 Jeep Grand Cherokee vehicles because a software error prevents the driver from knowing if a turn signal fails, increasing crash risk.

    Product
    JEEP — JEEP GRAND CHEROKEE 4XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V252000·2022-04-14

    Ford Recalls 2019 F-Series Trucks for Rearview Camera Defect

    Ford is recalling 2019 F-150, F-250, F-350, F-450, and F-550 trucks because a poor electrical connection may cause the rearview camera to display a blank or distorted image, increasing crash risk.

    Product
    FORD — FORD F-450 SD, F-350 SD, F-250 SD, F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22114·2022-04-14

    Rae Wellness Prenatal and Immunity Capsules Lack Child-Resistant Packaging

    Rae Wellness has recalled approximately 191,200 units of Prenatal and Immunity Capsules because the bottles do not have child-resistant packaging as required by law. The iron-containing supplements pose a risk of poisoning if swallowed by young children.

    Product
    Rae Prenatal Capsules and Rae Immunity Capsules
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V250000·2022-04-14

    Ford F-150 and related vehicles recalled for windshield wiper failure

    Ford is recalling 2020-2021 F-150s, Expeditions, Super Duties, and Lincoln Navigators with defective windshield wiper arms that may break and fail, reducing visibility and increasing crash risk. Owners should contact Ford at 1-866-436-7332 to schedule a free replacement.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR, F-550 SD, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22116·2022-04-14

    FAO Schwarz Toy Wood Play Smart Robot Buddy and Sensory Boards Recalled for Choking Hazard

    MerchSource is recalling about 46,200 FAO Schwarz Toy Wood Play Smart Robot Buddies and Sensory Boards because small parts can come loose, posing a choking hazard to young children.

    Product
    FAO Schwarz Toy Wood Play Smart Robot Buddy(s) and FAO Schwarz Toy Wood Sensory Boards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0759-2022·2022-04-13

    Pfizer Recalls Blood Pressure Tablets Due to Manufacturing Defects

    Pfizer is recalling quinapril HCl/hydrochlorothiazide tablets due to manufacturing defects that allowed N-nitroso impurities to exceed acceptable daily intake limits. Patients taking affected lots should contact their pharmacy.

    Product
    quinapril HCl/hydrochlorothiazide tablets, 20 mg/12.5 mg*, 90 Tablets bottles, Rx Only, Distributed by: Greenstone, LLC, Peapack, NJ, 07977, Made in Germany, NDC 59762-0220-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0892-2022·2022-04-13

    Unauthorized SARS-CoV-2 Antigen Tests recalled for lack of FDA clearance

    WHPM Inc. is recalling approximately 535,755 First SIGN SARS-CoV-2 Antigen Tests distributed in California, Florida, Louisiana, Massachusetts, and Texas. The tests were sold without FDA Emergency Use Authorization or clearance.

    Product
    First SIGN SARS-CoV-2 Antigen Test
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Food)·F-0966-2022·2022-04-13

    Bread Alone Fruit & Nut Sourdough recalled for undeclared sulfites

    Bread Alone, Inc. is recalling Fruit & Nut Sourdough bread because it contains undeclared sulfites. The affected product includes all loaves with expiration dates through March 28, 2022, distributed in New York, Massachusetts, and Connecticut.

    Product
    Bread Alone Fruit & Nut Sourdough; packaged in 27 ounce plastic bag
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0865-2022·2022-04-13

    Anterior Hip Surgical Kit Recall Due to Potential Sterility Breach

    Stradis Medical is recalling Anterior Hip Pack surgical kits due to perforated or torn outer bags that may compromise sterility. No illnesses have been reported.

    Product
    Anterior Hip Pack - Surgical Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V240000·2022-04-13

    2022-2023 BMW iX Air Bag Warning System Software Defect

    BMW is recalling 2022-2023 iX vehicles due to incorrect software in the air bag control unit. The malfunction indicator light may not illuminate if the air bag system has a problem, increasing crash injury risk.

    Product
    BMW — BMW IX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0963-2022·2022-04-13

    Caesar Dressing in 1.5 oz Pouch Recalled for Undeclared Soy Allergen

    Caesar dressing in 1.5 oz pouches manufactured by Sauer Brands Inc is being recalled due to undeclared soy. The product was distributed to institutional foodservice accounts in 14 states and poses a risk to people with soy allergies.

    Product
    Caesar dressing in a 1.5 oz pouch
    Category
    Food
    Distribution
    14 states
  • HighNHTSA·22V239000·2022-04-13

    Electronic Stability Control Software Defect in 2022 Toyota RAV4 Prime and Other Models

    Certain Toyota and Lexus vehicles may have a software defect preventing the Electronic Stability Control system from re-engaging after being manually disabled. Dealers will update the software free of charge.

    Product
    TOYOTA — TOYOTA, LEXUS SIENNA HYBRID, VENZA HYBRID, MIRAI, redundant VENZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0887-2022·2022-04-13

    Surgical drive mechanism recalled due to corrosion risk

    Maquet Cardiovascular is recalling the Ultima Activator II Reusable Drive Mechanism due to potential corrosion on pins, which could cause allergic reactions, metal toxicity, and other delayed health effects.

    Product
    Ultima Activator II Reusable Drive Mechanism, part # C-UA-5001. Labeled REF UA-5001.
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Drugs)·D-0754-2022·2022-04-13

    Pfizer recalls Accuretic blood pressure tablets for impurities exceeding acceptable limits

    Pfizer is recalling 53 bottles of Accuretic blood pressure tablets nationwide due to manufacturing impurities that exceed FDA acceptable daily intake limits. The affected lot is FG5379, expiring August 2024.

    Product
    Accuretic (quinapril HCl/hydrochlorothiazide) Tablets, 10 mg/12.5 mg*, 90 Tablets bottles, Rx Only, Distributed by: Parke-Davis, Division of Pfizer Inc, NY, NY 10017, Made in Germany, NDC 0071-3112-23.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0893-2022·2022-04-13

    SPECT/CT Imaging Systems Recalled Due to Defective Balancing Weight Bolts

    Siemens is recalling seven Symbia Intevo SPECT/CT imaging systems due to a quality defect in the bolts that secure the CT balancing weights, which could create a safety issue.

    Product
    Symbia Intevo Bold and Symbia Intevo 6 SPECT/CT Systems
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·22V244000·2022-04-13

    Nissan Recalls 2020 Sentra Vehicles for Headlight Misalignment

    Nissan is recalling 2020 Sentra vehicles with LED headlights because the right-hand headlight may be misaligned, potentially reducing visibility and increasing crash risk.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0880-2022·2022-04-13

    DeRoyal DEXMED Access Center Tray Recalled for Manufacturing Test Validation Uncertainty

    DeRoyal Industries is recalling 1,360 DEXMED ACCESS CENTER TRAY kits with Prevantics antiseptic swabs due to uncertain validation of manufacturing test methods. The affected kits were distributed in Florida, New Jersey, and Tennessee.

    Product
    DeRoyal DEXMED ACCESS CENTER TRAY, containing Prevantics antiseptic (chlorhexidine gluconate and isopropyl alcohol) swab, for preparation of the patient skin prior to surgery or injection.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Drugs)·D-0746-2022·2022-04-13

    Diabetes Drug Janumet Recalled Due to Stainless Steel Contamination

    Merck is recalling 3,600 cartons of Janumet (sitagliptin/metformin HCl) tablets nationwide due to the presence of stainless steel particulates in the tablets.

    Product
    JANUMET — JANUMET (SITAGLIPTIN AND METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide