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.

18101–18125 of 50404

  • HighUSDA FSIS·004-2022·2022-02-11

    Great American Cobbler Recalls Chicken Pot Pie for Undeclared Soy Allergen

    Great American Cobbler LLC is recalling Creole Style Chicken Pot Pie products because they contain soy, a known allergen, that is not declared on the label.

    Product
    Great American Cobbler Company LLC — Great American Cobbler Company, LLC, Recalls Creole Style Chicken Pot Pie Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    3 states
  • HighCPSC·22721·2022-02-10

    2022 Can-Am Outlander ATVs Recalled Due to Speedometer Crash Hazard

    BRP U.S. Inc. is recalling about 1,300 2022 Can-Am Outlander ATVs because the speedometer can display half the vehicle's true speed, creating a crash hazard. Consumers should stop using the vehicles and contact a Can-Am dealer for a free repair.

    Product
    2022 Can-Am Outlander ATVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22722·2022-02-10

    Serta Perfect Sleeper Mattresses Recalled for Fire Hazard

    Serta is recalling about 800 Perfect Sleeper mattresses because they fail to meet federal flammability standards, creating a fire hazard. No injuries have been reported.

    Product
    Serta® Perfect Sleeper® Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V076000·2022-02-10

    2022 Thor Motor Coach Motorhomes Rear Ladder Installation Defect Recall

    Thor Motor Coach is recalling 2022 ACE, Freedom Traveler, Hurricane, and Windsport motorhomes. The rear ladder may have been installed on the wrong side, which could break while in use and cause injury.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH ACE, FREEDOM TRAVELER, HURRICANE, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22078·2022-02-10

    WORX 13 Amp 1900 PSI Electric Pressure Washers Recalled for Hose Separation

    Positec USA is recalling about 17,630 WORX Brand 13 Amp 1900 PSI Electric Pressure Washers because the sprayer hose can separate from the spray wand during use, posing an impact injury hazard. Four minor injuries including cuts and bruises have been reported.

    Product
    WORX® Brand 13 Amp 1900 PSI Electric Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0552-2022·2022-02-09

    Premier Rotaclone Medical Device Recalled Due to Improper Storage Conditions

    Medline Industries is recalling 34 units of the Premier Rotaclone (Lot 696004N116) due to improper storage in temperature-controlled settings instead of required refrigeration. This may affect device performance or safety.

    Product
    Premier Rotaclone, Rx only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0627-2022·2022-02-09

    Delizza Chocolate Cream Puffs Recalled for Metal Contamination

    Delizza Belgian Mini Chocolate Cream Puffs are recalled due to small metal pieces found in the bakery's palm oil silo that could not be reliably detected by the manufacturer's metal detector system.

    Product
    Delizza BELGIAN MINI CHOCOLATE CREAM PUFFS NET WT. 14.1 oz (400g) 30 CREAM PUFFS PRODUCED IN THE US BY DELIZZA INCORPORATED 6610 CORPORATION PARKWAY, BATTLEBORO, NC 27809 UPC 6 76670 00402 2
    Category
    Food
    Distribution
    4 states
  • HighCPSC·22077·2022-02-09

    Home Easy Geek Heat Personal Heaters Recalled for Fire Hazard

    Home Easy is recalling about 3,000 Geek Heat DH-QN06 personal heaters because the toggle power switch can spark and cause a fire. The company has received three reports of fires caused by the switch, though no injuries or property damage have been reported.

    Product
    Personal Electric Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0540-2022·2022-02-09

    DIXI Microdeep Depth Electrode sterile barrier packaging defect

    DIXI Medical Microdeep Depth Electrodes are recalled due to potential deformation of the blister pack packaging that could compromise the sterile barrier. 345 units nationwide are affected.

    Product
    The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0534-2022·2022-02-09

    Microdeep Depth Brain Electrodes recall due to sterile barrier compromise risk

    DIXI Medical is recalling 484 Microdeep Depth Electrodes nationwide due to potential deformation of internal packaging that could compromise the sterile barrier of these brain recording devices.

    Product
    The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0545-2022·2022-02-09

    Cryptococcal Antigen Test Kits Recalled for Reduced Detection Specificity

    Immuno-Mycologics recalls 411 Cryptococcal Antigen test kits (lots F1021035, F1021036) for reduced specificity (90% vs. 99%), which may cause false-positive results leading to unnecessary anti-fungal therapy.

    Product
    CRYPTOCOCCAL ANTIGEN LATERAL FLOW ASSAY, IMMY, Lateral Flow Assay for the Detection of Cryptococcal Antigen in serum and CSF, REF CR2003, IVD, UDI: (01)00816387020919
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V073000·2022-02-09

    Mercedes-Benz Recalls 2021 Sprinter Vans for Incorrect Weight Labeling

    Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter vans because the gross vehicle weight rating may be incorrectly stated on the tire and loading label.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 3500, SPRINTER 2500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0535-2022·2022-02-09

    DIXI Medical Microdeep Depth Electrode Sterile Barrier Compromise Recall

    DIXI MEDICAL USA is recalling Microdeep Depth Electrodes used in neurological monitoring and stimulation due to potential deformation of the internal sterile packaging. The compromised sterile barrier could allow contamination before use.

    Product
    The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0553-2022·2022-02-09

    ARIES HSV 1&2 Diagnostic Cassettes May Leak, Affecting Test Results

    Luminex Corporation is recalling ARIES HSV 1&2 Assay cassettes (lot numbers AB3600A and AB3560A) due to a confirmed 0.9% leak rate. Leaking cassettes may cause incorrect or delayed test results.

    Product
    ARIES HSV 1&2 Assay, Catalog/REF# 50-10017
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0533-2022·2022-02-09

    Spinal Fusion Implant Insert Recalled for Assembly Defect

    XTANT Medical is recalling 24 units of the X060-0270 8mm Titanium Insert for the Axle Interspinous Fusion System due to a manufacturing defect that prevents proper assembly of crossbar plates. The defect could affect the device's function during spinal fusion procedures.

    Product
    X060-0270, 8mm Titanium Insert, Axle Interspinous Fusion System.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0555-2022·2022-02-09

    Young Dental Sterilization Indicator Labels May Contain Wrong Type

    YOUNG DH Dry Heat Indicator Labels used in healthcare sterilization may contain TTS Indicator Labels instead. Healthcare providers should verify package contents before use to ensure proper sterilization monitoring.

    Product
    YOUNG DH Dry Heat Indicators, PRESSURE SENSITIVE LABELS with COLOR INDICATOR STRIP, REF 116312 Intended for use by a health care provider to accompany products being sterilized through a sterilization procedure and to monitor one or more parameters of the sterilization…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0623-2022·2022-02-09

    Abby's Bakery frozen bread dough recalled due to glass contamination risk

    Abby's Bakery Homestyle White Bread Dough may contain glass fragments. The affected product (lots 21340-31 to 21340-36) should be discarded.

    Product
    Abbys Bakery Homestyle White Bread Dough. Product number 93596. Keep Frozen. 4-1 lb. loaves. Net Wt. 4 lbs. (1.81kg) UPC 40730-93596. Abby's Bakery, Wadena, MN 56482
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0549-2022·2022-02-09

    Philips eCareManager versions recalled due to unapproved Sentry Score software

    Philips is recalling certain versions of eCareManager software because the Sentry Score feature was not approved by FDA prior to distribution. Users should contact Philips for updated information.

    Product
    eCareManager version 4.2.1, eCareManager version 4.3.2, eCareManager version 4.3.3, eCareManager version 4.5.1, eCareManager version 4.5.2, eCareManager version 4.6.0- a software tool intended for use by trained medical staff providing supplemental remote support to bedside…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22073·2022-02-09

    Stack Em' Up Books Recalls Children's Stackable Toys for Excessive Lead Paint

    Stack Em' Up Books is recalling Adam the Apple children's stackable toys because the surface paint contains lead levels that exceed the federal lead paint ban. Lead is toxic if ingested by young children and can cause adverse health effects.

    Product
    Adam the Apple™ Children's Stackable Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0556-2022·2022-02-09

    Pelvic floor repair device may lack required packaging component

    FEMSelect Ltd is recalling 141 units of the EnPlace trans-vaginal pelvic floor repair system because certain lots may not have been packaged with the required Channel Tube Limiter accessory.

    Product
    The EnPlace is a single use trans-vaginal pelvic floor repair system which enables delivery of a tissue anchor to the ligaments of the vaginal cavity. The anchors are pre-loaded inside the device shaft and are ready for use. A thimble is also supplied, as an accessory for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0537-2022·2022-02-09

    DIXI Medical Microdeep Depth Electrode Packaging Defect Threatens Sterile Barrier

    DIXI MEDICAL USA is recalling Microdeep Depth Electrodes due to potential packaging deformation that could compromise the sterile barrier. Approximately 2,720 units were distributed nationwide for use in brain recording and stimulation procedures.

    Product
    The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V070000·2022-02-09

    2022 BMW X4 and Related Models Transmission Rollaway Risk Recall

    BMW is recalling certain 2022 330i, 530i, X3, and X4 vehicles because the transmission mechatronics unit may not have been properly assembled, potentially causing an internal leak that could lead to vehicle rollaway and crash risk.

    Product
    BMW — BMW X3, 330I, 530I, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0629-2022·2022-02-09

    Taste of Inspirations Creme Puffs Recalled Due to Metal Contamination

    Taste of Inspirations Creme Puffs are being recalled due to the potential presence of metal pieces in the product. The contamination was discovered in the bakery palm oil silo used during production.

    Product
    taste of Inspirations CREME PUFFS Whipped Cream Filled Pastry NET WT 13.2 OZ (375g) 30ct UPC: 7 25439 99597 9, DISTRIBUTED BY: DZA BRANDS, LLC SALISBURY, NC 28247
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0628-2022·2022-02-09

    Delizza Belgian Mini Cream Puffs Recalled Due to Metal Contamination

    Poppies International is recalling Delizza Belgian Mini Cream Puffs due to metal fragments found in the palm oil silo. The metal was not consistently detected during production screening.

    Product
    Delizza BELGIAN MINI CREAM PUFFS WHIPPED FILLING MADE WITH FRESH CREAM NET WT 13.2 oz (375g) PRODUCED IN THE US BY DELIZZA INCORPORATED 6610 CORPORATION PARKWAY, BATTLEBORO, NC 27809 UPC: 6 76670 00107 6, and NET WT. 3lb 5 oz. (1.5kg) 120ct UPC: 6 76670 00800 6
    Category
    Food
    Distribution
    4 states