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.

17401–17425 of 53124

  • HighFDA (Devices)·Z-1115-2022·2022-05-25

    Radiometer Arterial Blood Sampler recalled due to sterility guarantee loss

    Radiometer Medical is recalling Arterial Blood Samplers (REF:956-552) because sterility cannot be guaranteed throughout the product's shelf life. The recall affects 7,228 boxes distributed worldwide.

    Product
    Radiometer, REF:956-552, PIC050- Arterial Blood Sampler 1 X 2 mL, 80 IU electrolyte-balanced heparin. Not for injection. , IVD, Rx Only, Sterile EO, CE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0874-2022·2022-05-25

    Pfizer Accupril Blood Pressure Tablets Recalled for Nitrosamine Contamination

    Pfizer is recalling specific lots of Accupril (quinapril HCl) 40 mg tablets distributed nationwide and in Puerto Rico because the product contains N-nitrosoquinapril above acceptable limits, a manufacturing deviation.

    Product
    Accupril (Quinapril HCl Tablets) 40 mg, 90 Tablets, Rx only NDC 0071-0535-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1066-2022·2022-05-25

    Chocolate Sea Salt Caramels Recalled for Undeclared Soy Lecithin

    R & S Roberts Enterprises is recalling Milk & Dark Chocolate Sea Salt Healthy Bites because product labels do not declare soy lecithin used in the canola oil spray releasing agent. No illnesses have been reported.

    Product
    Milk & Dark Chocolate Sea Salt Healthy Bites. Chocolate coated caramels packaged bulk for stores. No UPC.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1083-2022·2022-05-25

    MicroScan WalkAway-40 plus Instrument recalled for incorrect AC power connector

    Beckman Coulter is recalling 22 MicroScan WalkAway-40 plus Instruments with an AC power entry connector rated at 1 ampere instead of the correct 10 amperes, creating a potential electrical hazard.

    Product
    MicroScan WalkAway-40 plus Instrument REF B1018-283
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1082-2022·2022-05-25

    EXALT Model D Single-Use Duodenoscope: Updated Instructions for Perforation Risk

    Boston Scientific issued updated instructions for the EXALT Model D Single-Use Duodenoscope to highlight the known risk of perforation and provide best practices for safe insertion, advancement, and removal.

    Product
    EXALT Model D Single-Use Duodenoscope (Box 2) UPN: M0054242CE1 Intended Use: sterile, single-use, flexible video duodenoscope intended for use with the EXALT" Controller to examine duodenum and perform various procedures within the duodenum including endoscopy and endoscopic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1108-2022·2022-05-25

    VitriGuard Cryopreservation Storage Device Recalled for Sterility Risk

    CooperSurgical is recalling 2,340 VitriGuard cryopreservation devices with compromised barrier seals that may compromise sterility. The affected devices were distributed across ten U.S. states.

    Product
    VITRIGUARD, CARRIER, CLEAR; Model. No. 43782001 The VitriGuard device is a cryopreservation storage device composed of a stick and cap.
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Food)·F-1070-2022·2022-05-25

    Gorton's Fish Sandwich Fillets Recalled Due to Bone Fragments

    Gorton's is recalling Fish Sandwich Fillets (18.3 oz) because they may contain large and/or sharp fish bones that could pose a choking hazard or cause injury.

    Product
    Gorton s Fish Sandwich Fillets, 18.3 OZ, UPC 44400 15440
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1073-2022·2022-05-25

    SE Grocers Cheesecake Sampler Recalled for Missing Pecan Allergen Declaration

    SE Grocers Cheesecake Sampler is recalled because pecans are not declared on the ingredient label, despite being processed during manufacturing, creating a risk for consumers with pecan allergies.

    Product
    SE Grocers Cheesecake SAMPLER New York Style, Chocolate Silk, Strawberry Swirl, Turtle - NO ARTIFICIAL FLAVORS - NET WT 32 OZ (2 LB) 907g - UPC 0 38259 13495 5 CONTAINS: EGG, MILK, SOY, AND WHEAT. MANUFACTURED IN A FACILITY THAT ALSO PROCESSES PEANUTS, TREE NUTS (ALMONDS…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1104-2022·2022-05-25

    HeartWare Ventricular Assist Device controller has translation errors in Finnish, Turkish

    HeartWare Ventricular Assist Device controllers in Finland and Turkey contain translation errors in displays, instructions, and patient manuals. The errors could affect proper device operation and emergency response.

    Product
    HeartWare Ventricular Assist Device (HVAD) System Controller, Model Number 1420
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0883-2022·2022-05-25

    Trulicity Injection Recalled Due to Temperature Exposure During Shipment

    A batch of Trulicity (dulaglutide) injection was recalled due to temperature exposure during distribution in New Mexico. The product was exposed to temperatures outside its labeled storage requirements due to inclement weather.

    Product
    Trulicity (dulaglutide) injection, 1.5 mg/0.5mL once weekly, 4 Single-Dose Pens, Rx only, Eli Lilly and Company, Indianapolis, IN 46285, NDC 00002-1434-80
    Category
    Drug
    Distribution
    1 state
  • HighNHTSA·22V372000·2022-05-24

    E-One Recalls 2022 Fire Trucks Due to Lighting Failure Risk

    E-One Incorporated is recalling 2022 Commercial, Cyclone 2, Cyclone N, and Typhoon N fire trucks because a defective circuit board can cause vehicle lighting to fail.

    Product
    E-ONE — E-ONE COMMERCIAL, CYCLONE II, CYCLONE N, TYPHOON N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V373000·2022-05-24

    Spartan Fire Recalls Fire Trucks Due to Lighting Failure Risk

    Spartan Fire is recalling 2021-2023 fire trucks because a defective circuit board can cause lighting to fail, increasing crash risk.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, FC-94, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E043000·2022-05-23

    Curt Retrac Maglatch Bracket Kits Recalled for Potential Fracture

    Lippert is recalling Curt Retrac Maglatch Bracket Kits for 2021 Kenworth and Peterbilt trucks because the metal may fracture, risking grill guard damage and crashes.

    Product
    STRUCTURE:BODY:BUMPERS:ACTIVE SHUTTERS/GRILL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V368000·2022-05-23

    Audi Recalls 2022 A4, A6, and Q5 Models for Engine Control Unit Defect

    Volkswagen Group of America is recalling 2022 Audi A4, A6, and Q5 Sportback vehicles because a semiconductor in the engine control unit may short-circuit, causing the engine to stall and increasing crash risk.

    Product
    AUDI — AUDI A4, A6, Q5 SPORTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E042000·2022-05-23

    Red Rock Recalls Swing Up Table Bases Due to Incomplete Welds

    Red Rock LLC is recalling 944 Swing Up Table Bases because incomplete welds may cause the table to drop unexpectedly, increasing the risk of injury.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V361000·2022-05-20

    2021-2022 Coachmen motorhomes recalled for cooktop gas leak risk

    Forest River is recalling 2021-2022 Coachmen motorhomes with defective cooktop burner valves that can develop gas leaks. The leaks pose a fire risk and will be remedied by free cooktop replacement.

    Product
    COACHMEN — COACHMEN NOVA, BEYOND, GALLERIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V360000·2022-05-20

    Daimler Recalls 2019-2021 Sprinter Vehicles for eCall Software Defect

    Daimler Vans USA is recalling 2019-2021 Freightliner and Mercedes-Benz Sprinter vehicles because a software error may disable the emergency call system.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 2500, SPRINTER 3500, SPRINTER 4500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V364000·2022-05-20

    GM Recalls 2022 Chevrolet HD Trucks for Brake Fluid Leak Risk

    General Motors is recalling 2022 Chevrolet 4500HD, 5500HD, and 6500HD trucks because a brake line fitting may leak fluid, increasing stopping distance.

    Product
    CHEVROLET — CHEVROLET 6500HD, 5500HD, 4500HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V365000·2022-05-20

    Mercedes-Benz Vehicles: Emergency Calling System Disabled by Software Error

    Mercedes-Benz USA is recalling certain 2017-2022 models after a communication module software error disabled the emergency eCall system. Owners can receive a free software update via over-the-air delivery or at a dealer.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH E 350, E 450, CLA 250, SLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V359000·2022-05-19

    2022 Chevrolet Blazer driver's seat frame weld defect

    General Motors is recalling certain 2022 Chevrolet Blazer vehicles due to an improper weld in the driver's seat cushion frame that may fail to adequately restrain the driver in a crash.

    Product
    CHEVROLET — CHEVROLET, CADILLAC MALIBU, EQUINOX, XT4, BLAZER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V358000·2022-05-19

    Coach House motorhomes recalled for cooktop gas leak fire risk

    Coach House is recalling certain 2021-2022 Platinum, Platinum II, and Arriva motorhomes with cooktop burner control valves that may leak gas and increase fire risk. Dealers will replace the cooktop at no cost.

    Product
    COACH HOUSE — COACH HOUSE PLATINUM II, PLATINUM, ARRIVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1057-2022·2022-05-18

    Chemotherapy Infusion Bag Adaptor May Disconnect and Spill Hazardous Drugs

    Simplivia Healthcare is recalling OnGuard2 CSTD Bag Adaptors because they may disconnect from infusion bags, potentially spilling hazardous medications.

    Product
    OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1043-2022·2022-05-18

    Medtronic IN.PACT AV Balloon Catheter: Damaged Packaging May Affect Sterility

    Medtronic is recalling IN.PACT AV paclitaxel-coated balloon catheters because packaging damage may result in loss of sterility. The devices were distributed worldwide and in the United States.

    Product
    Medtronic IN.PACT AV, Paclitaxel-coated PTA Balloon Catheter, REF: IAV06008008P, Sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1059-2022·2022-05-18

    VITEK 2 Systems Software Issue May Produce Incorrect Antibiotic Test Results

    bioMerieux VITEK 2 bacterial identification systems have a software defect where antibiotic susceptibility and synergy test results transmitted to laboratory systems may omit user or automated corrections, potentially leading to incorrect test interpretation.

    Product
    VITEK 2 Systems and VITEK 2 with MYLA.
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·22V352000·2022-05-18

    Can-Am Recalls 2015-2019 Spyder RT and F3 for Sprocket Defect

    Bombardier is recalling 2015-2019 Can-Am Spyder RT and F3 motorcycles because a defective front sprocket may wear prematurely, causing a loss of drive power and increasing crash risk.

    Product
    CAN-AM — CAN-AM SPYDER RT, SPYDER F3
    Category
    Vehicle
    Distribution
    Distributed nationwide