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.

15226–15250 of 53092

  • HighFDA (Devices)·Z-0343-2023·2022-12-07

    Surgical Gown Recall Due to Potential Open Seal Pouches Affecting Sterility

    Owens & Minor Distribution recalls Aero Blue Performance Surgical Gowns due to potential open seal pouches that could compromise sterility and result in non-sterile products being used in surgery.

    Product
    Aero Blue Performance Surgical Gown, XL- Sterile surgical gown Code: 41734
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0347-2023·2022-12-07

    Medical laboratory reagent recalled for potential false-negative test results

    Greer Laboratories recalled a hypersensitivity pneumonitis test reagent (Lot 389591) due to decreased reactivity that could cause false-negative results. The issue affects 218 units distributed across 12 U.S. states and two countries.

    Product
    GREER M. FAENI, 0.25 mL 20 MG/ML, Item: K6, Analyte Specific Reagent, HYPERSENSITIVITY PNEUMONITIS test system, gel diffusion kit for demonstrating precipitating antibodies.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-0344-2023·2022-12-07

    Mobile CT Scanner Battery Fire Risk in Units With Bypassed Monitoring

    Mobius Imaging is recalling MobiCT-32 AIRO Mobile CT Scanner units due to a reported battery fire in devices where battery monitoring systems were bypassed. The affected units' batteries must be replaced.

    Product
    MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography (CT) system, software version 2.1.1
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-0181-2023·2022-12-07

    Fudgeamentals Chocolate Fudge Bites recalled for undeclared tree nuts

    Fudgeamentals Chocolate Fudge Bites (8 oz) are being recalled because they contain undeclared tree nuts. Consumers with tree-nut allergies are at risk of allergic reaction.

    Product
    Fudgeamentals Chocolate Fudge Bites (8 oz); packaged in clear plastic container
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0346-2023·2022-12-07

    Diagnostic Kit Recalled for False Positive Bacterial Identification Results

    Accelerate Diagnostics is recalling the Accelerate PhenoTest BC kit due to improperly formulated FISH probes that produce false positive identification results for Staphylococcus aureus and Streptococcus species. Approximately 7,160 kits have been distributed across the United States and internationally.

    Product
    Accelerate PhenoTest BC kit REF 10102018
    Category
    Medical Device
    Distribution
    31 states
  • HighFDA (Devices)·Z-0345-2023·2022-12-07

    Accelerate PhenoTest BC Kit Recall Due to False Positive Bacterial Identification

    Accelerate Diagnostics is recalling 200 kits of the Accelerate PhenoTest BC diagnostic test due to improperly formulated FISH probes that may produce false positive results for Staphylococcus aureus and Streptococcus bacteria.

    Product
    Accelerate PhenoTest BC kit REF 10101018
    Category
    Medical Device
    Distribution
    31 states
  • HighFDA (Devices)·Z-0340-2023·2022-12-07

    Intuitive Da Vinci Stapler Instruments Recalled for Potential Staple Deployment Failure

    Intuitive Surgical is recalling Da Vinci Xi surgical stapling instruments due to potential staple deployment failure and device fragment generation. No injuries have been reported.

    Product
    INTUITIVE Da Vinci Xi 8mm SureForm 30 Curved-Tip Stapler Da Vinci Xi|X REF 488530 INTUITIVE Da Vinci 8mm SureForm 30 Reload 30 mm Gray 4-Row 2.0 mm Xi|X REF 48230M INTUITIVE Da Vinci 8mm SureForm 30 Reload 30 mm White 4-Row 2.5 mm Xi|X REF 48230W INTUITIVE Da Vinci 8mm…
    Category
    Medical Device
    Distribution
    24 states
  • HighFDA (Devices)·Z-0342-2023·2022-12-07

    CMV IgM EIA Diagnostic Test Recalled for Increased False Positives

    Bio-Rad Laboratories is recalling 180 CMV IgM EIA diagnostic test kits due to unusually high rates of false positive results. The recall affects test kits distributed in 14 U.S. states.

    Product
    CMV IgM EIA, in vitro diagnostic.
    Category
    Medical Device
    Distribution
    14 states
  • HighNHTSA·22V902000·2022-12-07

    Nova Bus Recalls LFS Models for Non-Standard Auxiliary Lighting

    Nova Bus is recalling 2009-2021 LFS and LFS Artic transit buses because non-standard color auxiliary lights may distract other drivers and increase crash risk.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0072-2023·2022-12-07

    FDA recalls prescription desmopressin acetate tablets for subpotency

    Heritage Pharmaceuticals' desmopressin acetate tablets (0.2mg) have been recalled nationwide due to subpotency. The voluntary recall affects 13,805 bottles; no illnesses have been reported.

    Product
    DESMOPRESSIN ACETATE — DESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0348-2023·2022-12-07

    Medical device test system recalled for decreased reactivity and false-negative results

    Greer Laboratories recalled a hypersensitivity pneumonitis test kit (102 units, Lot 389592) after stability testing revealed decreased reactivity that could cause false-negative results. The issue was discovered in October 2021.

    Product
    GREER DIA - KIT ANTIGEN M. FAENI, 2.0mL 20 MG/ML, Analyte Specific Reagent, Item: K62, HYPERSENSITIVITY PNEUMONITIS test system, gel diffusion kit for demonstrating precipitating antibodies.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Food)·F-0180-2023·2022-12-07

    Amy's Kitchen Gluten Free Bean and Cheese Burritos Recalled for Plastic Contamination

    Amy's Kitchen is recalling Gluten Free Bean and Cheese Burritos (Lot 30H0922, best before 08/2024) due to potential plastic pieces in the product. Approximately 5,134 cases were distributed to 18 U.S. states.

    Product
    Amy's Kitchen Gluten Free Bean and Cheese Burrito 5.5 oz. individually wrapped plastic packages - 12 units per case UPC - 042272-00353-2 Frozen INGREDIENTS: ORGANIC PINTO BEANS, FILTERED WATER, ORGANIC BROWN RICE, ORGANIC GARBANZO BEAN FLOUR, ORGANIC TOMATO PUR¿E, WHITE CHEDDAR…
    Category
    Food
    Distribution
    18 states
  • HighFDA (Drugs)·D-0071-2023·2022-12-07

    Daytrana transdermal methylphenidate patches recalled for adhesive defect

    Noven Pharmaceuticals recalls 3,977 boxes of Daytrana methylphenidate transdermal patches nationwide due to defective adhesive properties in lot 91316. Affected patches may fail to adhere properly or deliver medication inconsistently.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V898000·2022-12-06

    Hino Recalls 2022-2023 Trucks Due to Fuel Pickup Tube Defect

    Hino is recalling 970 specific 2022-2023 models because a fuel tube may restrict fuel flow, potentially causing engine stalls and increasing crash risk.

    Product
    HINO — HINO NJ7A, NJ7B, NV7A, NE7A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V900000·2022-12-06

    KTM 1290 Super Duke R Motorcycles Recalled for Electrical Wiring Defect

    KTM is recalling 2020-2022 1290 Super Duke R motorcycles because the main wiring harness may be misrouted or missing parts, potentially causing an electrical short-circuit and engine stall.

    Product
    KTM — KTM 1290 SUPER DUKE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V896000·2022-12-06

    Volvo Recalls 2022-2023 VNL Vehicles for Air Tank Bracket Defect

    Volvo Trucks is recalling certain 2022-2023 VNL vehicles because excessively tightened air tank bracket fasteners may break, allowing the air tank to detach and become a road hazard.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-12052022-001·2022-12-05

    Ground Beef Alert Issued for E. Coli O157:H7 Contamination at Texas Store

    USDA FSIS issued a public health alert for ground beef sold at La Michoacana Meat Market in Greenville, Texas, after testing positive for E. coli O157:H7.

    Product
    FSIS Issues Public Health Alert for Ground Beef Products That Tested Positive for E. Coli O157:H7
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·22V894000·2022-12-05

    Old School Trailers Recalls 2022 Models Due to Awning Seam Defect

    Old School Trailers is recalling 2022 models because a welded seam on the electric retractable awning may separate, causing the awning to drop and increasing injury risk.

    Product
    OLD SCHOOL TRAILERS — OLD SCHOOL TRAILERS OLD SCHOOL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23713·2022-12-01

    Kubota RTV-XG850 Utility Vehicles Recall for Steering Shaft Failure

    Kubota is recalling about 19,500 RTV-XG850 utility vehicles because the steering shaft can shear near the power steering housing, causing loss of steering control. No injuries or deaths have been reported.

    Product
    Kubota RTV-XG850 Model Utility Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23712·2022-12-01

    Polaris RZR Pro XP 4 Vehicles Recalled Due to Fire Hazard

    Polaris is recalling about 600 model year 2021-2022 RZR Pro XP 4 recreational off-road vehicles because a fuel leak at the fuel pump assembly joint can occur near a hot surface, creating a fire hazard. The company has received five reports of fuel leaks, including one report of fire, but no injuries have been reported.

    Product
    Model Years 2021-2022 RZR Pro XP 4 Recreational Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23056·2022-12-01

    Cuisinart Compact Blender and Juice Extractor Combos Recalled for Laceration Hazard

    Conair is recalling about 66,000 Cuisinart Compact Blender & Juice Extractor Combos (Model CBJ-450) because the nut holding the blender blade assembly can loosen and detach during use, creating a laceration hazard.

    Product
    Cuisinart Compact Blender & Juice Extractor Combos Model CBJ-450
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23715·2022-12-01

    2022 Honda TRX90X ATVs Recalled Due to Stuck Throttle Cable

    American Honda is recalling about 2,900 2022 model year TRX90X ATVs because the throttle cable can get stuck, creating a crash and injury hazard. Consumers should stop using the vehicles and contact an authorized Honda Powersports dealer for a free inspection and repair.

    Product
    2022 model year Honda TRX90X ATVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23059·2022-12-01

    JBR Solutions Recalls Aduro Surge Protectors for Shock and Fire Hazards

    JBR Solutions is recalling about 51,750 Aduro surge protectors due to incorrect polarization and poorly soldered connections that pose shock and fire hazards. No injuries or fires have been reported.

    Product
    Aduro surge protectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23058·2022-12-01

    The Laundress cleaning products recalled for bacterial contamination

    The Laundress is recalling approximately 8 million laundry and household cleaning products that may contain harmful bacteria including Burkholderia cepacia complex, Klebsiella aerogenes, and Pseudomonas species. People with weakened immune systems or underlying lung conditions face risk of serious infection.

    Product
    The Laundress laundry and household cleaning products
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23714·2022-12-01

    HABA USA Recalls Discovery Cubes Animal Hide and Seek Activity Toys

    HABA USA is recalling about 800 Discovery Cubes Animal Hide and Seek activity toys because the seam on the toy's house can open, allowing access to filling that poses choking and ingestion hazards for young children. No injuries have been reported.

    Product
    Discovery Cubes Animal Hide and Seek Activity Toy
    Category
    Consumer Product
    Distribution
    Distributed nationwide