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.

20701–20725 of 50413

  • HighNHTSA·21V252000·2021-04-10

    Spartan Fire Recalls 2019-2021 Gladiator and MetroStar for Steering Defect

    Spartan Fire is recalling 2019-2021 Gladiator and MetroStar vehicles because pressure in the power steering pump may break the shaft seal, causing a loss of steering assist.

    Product
    SPARTAN FIRE — SPARTAN FIRE GLADIATOR, METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V250000·2021-04-09

    Keystone Bullet RV trailers recalled for defective emergency window handle

    Keystone is recalling certain 2020-2021 Bullet trailers with defective bedroom emergency egress windows. An incorrect crank handle may make the window difficult to open in an emergency.

    Product
    KEYSTONE — KEYSTONE BULLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V245000·2021-04-08

    GM Recalls 2014-2016 Trucks and SUVs for Seat Belt Cable Defect

    General Motors is recalling specific 2014-2016 Chevrolet and GMC vehicles because a driver's seat belt cable may break, reducing safety protection.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 1500, TAHOE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21736·2021-04-08

    GEO Essential Oils Recalled for Non-Child-Resistant Packaging and Poisoning Risk

    Geo Essential LLC is recalling Wintergreen and Alleviate essential oils because the packaging is not child-resistant, posing a poisoning risk to young children.

    Product
    GEO Wintergreen Organic Essential Oil and GEO Alleviate Organic Essential Oil Blend
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V243000·2021-04-07

    Utility Trailer Recalls VS2DC, VS2DX, VS3DX Models for Missing Weld

    Utility Trailer is recalling 2006-2021 VS2DC, VS2DX, and VS3DX trailers because a missing weld may cause the slider rail to detach, increasing crash risk.

    Product
    UTILITY TRAILER — UTILITY TRAILER VS3DX, VS2DX, VS2DC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1330-2021·2021-04-07

    Siemens ACUSON Sequoia Ultrasound Systems Recalled for Incorrect Delivery Date Calculations

    Siemens is recalling 1,172 ACUSON Sequoia ultrasound systems because a software error may calculate incorrect Estimated Dates of Delivery, potentially influencing clinical decisions.

    Product
    Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Food)·F-0365-2021·2021-04-07

    Blanxart Milk Chocolate with Hazelnuts Recalled for Metal Fragment

    Culinary Collective is recalling Blanxart Milk Chocolate with Hazelnuts because a small metal fragment was found inside a bar.

    Product
    Blanxart Milk Chocolate with Hazelnuts Cacao 33% Min. Net wt.7 oz. Product is packaged with paper and internal foil wrapper. UPC 6 66785 20322 9. The label is read in parts: "***BLANXART Milk Chocolate with Hazelnuts CACAO 33% *** BB Chocolate Grup, S.A Tambor del Bruc 13 08970…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0369-2021·2021-04-07

    Caribou Coffee Turkey Sandwich Recalled for Listeria Contamination Risk

    J & J Distributing Company is recalling Caribou Coffee Turkey Sandwiches due to potential Listeria monocytogenes contamination. The product was distributed to 46 retail locations in eight states.

    Product
    Caribou Coffee Turkey Sandwich, Net Wt. 9.0oz. (255g)
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1323-2021·2021-04-07

    Nuvasive PRECICE STRYDE Intramedullary Nail Recall for Biological Safety Concerns

    Nuvasive Specialized Orthopedics is recalling PRECICE STRYDE intramedullary nails due to complaints of adverse events potentially related to biological safety, including pain and bony abnormalities.

    Product
    PRECICE STRYDE - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21103·2021-04-07

    Epicure Recalls Glass Prep Bowls Due to Laceration Hazard

    Epicure is recalling glass prep bowls that may shatter during use, posing a laceration hazard. Consumers should stop using the product and contact Epicure for a free replacement.

    Product
    Epicure Prep Bowls (Set of Four)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0317-2021·2021-04-07

    Ferring Recalls ZOMA-Jet 5 Demonstration Kits Due to Defective Delivery System

    Ferring Pharmaceuticals is recalling 301 ZOMA-Jet 5 Demonstration Kits because the injector pen may break apart and disintegrate into pieces.

    Product
    ZOMA-Jet 5 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 5mg vial, Rx only, ZOMA-Jet 5 Demonstration Kit contains -ZOMA-Jet 5 device - 5 Needle-Free Head A's - 2 Vial Adaptors - 1 Carrying Case - 1 User Manual; Manufactured for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0380-2021·2021-04-07

    Land O'Lakes Queso Dip Recalled for Potential Metal Foreign Material

    Land O'Lakes is recalling Queso Bravo White Cheese Dip because it may contain metal foreign material. Consumers should stop using the product.

    Product
    Land O Lakes Queso Bravo White Cheese Dip with Jalapeno and Red Peppers. Net Wt 5 lbs. (2.26kg), UPC 34500-48238. Shipping Case: 6 - 5 lb Pouches. Net Wt. 20.00 Lbs. (13.60 kg) Item Code 48238000034500
    Category
    Food
    Distribution
    20 states
  • HighFDA (Food)·F-0371-2021·2021-04-07

    Earthgrown Mini Taco Dip Recalled for Listeria Contamination Risk

    J & J Distributing Company is recalling Earthgrown Mini Taco Dip due to potential Listeria monocytogenes contamination. The product was distributed to 46 retail locations in eight states.

    Product
    Earthgrown Mini Taco Dip, Net Wt. 8oz. (227g), UPC 6 10014 22341 0, Packed By J&J Distributing Inc. 653 Rice St, St Paul, MN 55103
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1318-2021·2021-04-07

    EPIX Therapeutics Recalls DiamondTemp Ablation Catheters Due to Labeling Errors

    EPIX Therapeutics is recalling 60 units of DiamondTemp Unidirectional Large Curve Ablation Catheters because packaging and instructions list incorrect catheter sizes, posing a risk of blood clots or air emboli.

    Product
    EPIX Therapeutics DiamondTemp Unidirectional Large Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF: CEDT200L, Sterile EO, UDI: 00812499030259
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·21102·2021-04-07

    RH Recalls Children's Bath Wraps for Flammability Standard Violations

    RH is recalling approximately 55,700 children's bath wraps in the U.S. because they fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries.

    Product
    Animal, Heathered Plush and Luxe Sherpa Children's Bath Wraps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0375-2021·2021-04-07

    J & J Distributing Recalls Taco Dip for Listeria Risk

    J & J Distributing Company is recalling 8-ounce Kwik Trip Taco Dip due to potential Listeria monocytogenes contamination. The product was distributed to 46 retail locations in eight states.

    Product
    Taco Dip [Kwik Trip], Net Wt. 8oz (227g), UPC 0 38232 36091 3, Distributed By H. Brooks & Co. Mpls MN 55112
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-0372-2021·2021-04-07

    Haug Fresh Mini 7 Layer Dip Tray Recalled for Listeria Risk

    J & J Distributing Company is recalling Haug Fresh Mini 7 Layer Dip Trays due to potential Listeria monocytogenes contamination.

    Product
    Haug Fresh Mini 7 Layer Dip Tray, Net Wt. 22oz (624g), UPC 6 10014 16414 0, Packed and Distributed by J&J Distributing, St Paul Mn 55103
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1320-2021·2021-04-07

    EPIX Therapeutics Recalls DiamondTemp Ablation Catheters Due to Labeling Errors

    EPIX Therapeutics is recalling 18 units of DiamondTemp Bidirectional Large Curve Ablation Catheters because packaging and instructions list incorrect sizes, posing a risk of blood clots or air emboli.

    Product
    EPIX Therapeutics DiamondTemp Bidrectional Large Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:CEDTB400L, SterileEO, UDI: 00812499030303
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1324-2021·2021-04-07

    Nuvasive Precice Bone Transport Nail Recalled for Biological Safety Concerns

    Nuvasive Specialized Orthopedics is recalling 226 Precice Bone Transport nails due to complaints of pain and bony abnormalities related to biological safety.

    Product
    Precice Bone Transport - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0373-2021·2021-04-07

    Fresh Thyme Taco Dip Recalled for Listeria Contamination

    Fresh Thyme Taco Dip (10oz) is recalled due to potential Listeria monocytogenes contamination. The product was distributed to 46 retail locations in 8 states.

    Product
    Fresh Thyme Taco Dip, Net Wt. 10oz (283g), UPC 8 41330 12368 3
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-0354-2021·2021-04-07

    BakeryWorks Recalls UnTortillas Grain Free for Potential Undeclared Egg

    BakeryWorks LLC is recalling UnTortillas Grain Free tortillas because they may contain undeclared egg. The recall affects 471 cases distributed in Chicago, IL.

    Product
    UnTortillas Grain Free * 3 g of non-fibre carbs * 210g 6 tortillas per bag, 8 packages per case. UPC# 40628250179024 packaged in flexible plastic
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1328-2021·2021-04-07

    Alcon Custom Ophthalmic Surgical Procedure Packs Recalled for Mold

    Alcon is recalling 249,853 custom ophthalmic surgical procedure packs because mold was found on gowns included in the packages.

    Product
    Alcon Custom Ophthalmic Surgical Procedure Packs
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0370-2021·2021-04-07

    Tastebuds Taco Platter Recalled for Listeria monocytogenes Contamination Risk

    J & J Distributing Company is recalling Tastebuds Taco Platters due to potential Listeria monocytogenes contamination. The product was distributed to retail locations in eight states.

    Product
    tastebuds Taco Platter, Net Wt. 26oz. (738g), UPC 0 38232 31683 5; Net Wt. 15.8oz (448g), UPC 0 38232 33235 4, Distributed By H. Brooks & Co Mpls MN 55112
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1317-2021·2021-04-07

    EPIX Therapeutics Recalls DiamondTemp Ablation Catheters Due to Labeling Errors

    EPIX Therapeutics is recalling 100 units of DiamondTemp Unidirectional Small Curve Ablation Catheters because packaging and instructions list incorrect catheter sizes, posing a risk of blood clots or air emboli.

    Product
    EPIX Therapeutics DiamondTemp Unidirectional Small Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF CEDT100S, SterileEO, UDI 00812499030198
    Category
    Medical Device
    Distribution
    0 states