The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

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.

9101–9125 of 29123

  • SevereFDA (Food)·F-1585-2020·2020-10-07

    Spokane Produce Recalls Pico De Gallo Salsa Due to Salmonella Risk

    Spokane Produce, Inc. is recalling two items of refrigerated Pico De Gallo Salsa Hot because they contain onion supplied from Thomson International, Inc. that may be contaminated with Salmonella Newport.

    Product
    Item 83985 Pico De Gallo Salsa Hot, Refrigerated, net wt. 8 OZ, packaged in Plastic Container. Item 83986 Pico De Gallo Salsa Hot Saddlin' Up, Refrigerated, net wt. 16 OZ, packaged in Plastic Container.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1551-2020·2020-10-07

    Spokane Produce Potato Salad Recalled for Salmonella Newport Risk

    Spokane Produce, Inc. is recalling refrigerated potato salad containing onion supplied by Thomson International, Inc. due to a Salmonella Newport risk.

    Product
    Item 80698 Potato Salad, Refrigerated, net wt. 9 OZ, packaged in Cardboard Box.
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·20V618000·2020-10-07

    Lamborghini Recalls 2020 Aventador SVJ Models for Suspension Bolt Issue

    Lamborghini is recalling 2020 Aventador SVJ Coupe and Roadster vehicles because loose front suspension anchor bolts may cause a loss of vehicle control.

    Product
    LAMBORGHINI — LAMBORGHINI AVENTADOR SVJ ROADSTER, AVENTADOR SVJ COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1578-2020·2020-10-07

    Spokane Produce Recalls Fresh Medium Salsa Due to Salmonella Newport Risk

    Spokane Produce, Inc. is recalling 8-ounce containers of Fresh Medium Salsa because the product contains onion supplied by Thomson International, Inc., which is associated with Salmonella Newport.

    Product
    Item 84023 Fresh Medium Salsa, Refrigerated, net wt. 8 OZ, packaged in Plastic Container.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0026-2021·2020-10-07

    ASSURED Hand Sanitizer Recalled for CGMP Deviations and Methanol Risk

    4e Brands North America is recalling ASSURED Instant Hand Sanitizer due to manufacturing in a facility associated with methanol contamination, representing poor CGMPs.

    Product
    ASSURED Instant Hand Sanitizer Vitamin E and Aloe, (70% ethyl alcohol), Packaged as a) 8 fL oz / 236 ml bottle, UPC 6 39277 49069 8 b) 10 fL oz / 296 ml bottle, UPC 6 39277 49069 8, Distributed by Geenbrier International, Inc., 500 Volvo Parkway, Chesapeake, VA 23320, Made in Mex
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0049-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 9,214 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" C-13 Cutting SV2298, UDI: 20884521151021 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in liga
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0044-2021·2020-10-07

    Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 1,266 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. The defect could compromise the sterile field and increase the risk of surgical site infections.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 18" P-12 Cutting SV497G, UDI: 20884521149707 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in liga
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0023-2021·2020-10-07

    Blumen Hand Sanitizer Recalled for CGMP Deviations and Methanol Risk

    4e Brands North America is recalling Blumen Advanced Hand Sanitizer due to manufacturing in a facility associated with methanol contamination.

    Product
    blumen ADVANCED HAND SANITIZER, 70% ALCOHOL CONTENT, (70% ethyl alcohol), packaged as a) 3.4 fl oz / 100 ml bottle, UPC 8 14266 02359 4 b) 7.5 fl. oz./221 ml bottle, UPC 8 14266 02362 4 b) 33.8 fl. oz./1L bottle, UPC 8 14266 02369 3, Distributed in USA and Canada By: 4e Brands No
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V614000·2020-10-06

    Ferrari Recalls 812 Superfast Vehicles for Rear Window Adhesion Defect

    Ferrari is recalling 2018-2020 812 Superfast vehicles because the rear window may have been bonded incorrectly, potentially leading to detachment and increased crash risk.

    Product
    FERRARI — FERRARI 812 SUPERFAST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V607000·2020-10-02

    Mercedes-Benz Recalls 2020 GLC 350e for High-Voltage Wiring Harness Defect

    Mercedes-Benz is recalling 2020 GLC 350e hybrid vehicles because a high-voltage wiring harness shield may fail, causing an electrical malfunction and vehicle stall.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 350 E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V610000·2020-10-02

    Micro Bird Recalls 2019 MB II Buses Due to Electrical Fire Risk

    Micro Bird is recalling 75 model-year 2019 MB II buses because a grounding wire issue may cause a short circuit, increasing the risk of fire.

    Product
    MICRO BIRD — MICRO BIRD MB II SCHOOL BUS, MB II TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V603000·2020-10-01

    GM Recalls 2018 Trucks and SUVs for Brake Assist Defect

    General Motors is recalling 2018 Cadillac, Chevrolet, and GMC vehicles because a vacuum pump issue can reduce power brake assist, increasing stopping distance.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, GMC SILVERADO 1500, ESCALADE, TAHOE, SIERRA 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0006-2021·2020-09-30

    Toufayan Bakery Recalls Gluten-Free Animal Crackers Due to Undeclared Wheat

    Toufayan Bakery, Inc. is recalling Goodie Girl Gluten Free Magical Animal Crackers because the product was mixed with wheat-containing product, resulting in undeclared wheat.

    Product
    Goodie Girl, Gluten Free Magical Animal Crackers, 7 ounce , paper cartons, 6 packages per case, Best By JAN 11 21 A3
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·20V599000·2020-09-30

    Ford Recalls 2020 F-350 Trucks Due to Rear Axle Mismatch

    Ford is recalling 2020 F-350 trucks with ambulance prep packages because incorrect rear axles were installed, creating a risk of tire blowouts.

    Product
    FORD — FORD redundant F-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1527-2020·2020-09-30

    Lay's Barbecue Potato Chips Recalled for Undeclared Milk

    Frito-Lay is recalling specific bags of Lay's Barbecue Flavored Potato Chips because they may contain undeclared milk.

    Product
    Lay's Barbecue Flavored Potato Chips 1 oz. UPC 28400 00861; Lay's Barbecue Flavored Potato Chips 1 1/2 oz. UPC 28400 00300; Lay's Barbecue Flavored Potato Chips 2 5/8 oz. UPC 28400 32420; Lay's Barbecue Flavored Potato Chips 7 3/4 oz. UPC 28400 19961; Lay's Barbecue Flavored
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-1532-2020·2020-09-30

    Frito-Lay Classic Variety Mix Recalled for Undeclared Milk

    Frito-Lay is recalling 1,236 bags of Classic Variety Mix and Classic Mix due to potential undeclared milk. The products were distributed to retail and foodservice channels in 11 western states.

    Product
    Frito-Lay 30 count Classic Variety Mix tray Carton UPC 000 28400 52347 9, 1 1/2 oz. individual bags packaged in a larger tray AND Frito-Lay 30 count Classic Mix cube box UPC 28400 06241, 1 oz. individual bags packaged in a larger box
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-1544-2020·2020-09-30

    Gilster-Mary Lee Recalls Organic Microwave Popcorn Due to Glass Contamination

    Gilster-Mary Lee Corp. is recalling specific brands of organic microwave popcorn because tempered glass pieces were found in the product.

    Product
    Microwave popcorn packaged in the following ways: 1) Full Circle Organic Microwave Popcorn Salted, 3-2.9 oz (82 g) bags, Net Wt. 8.7 oz (247 g), Distributed by Topco Associates LLC, Elk Grove Villiage, IL, UPC 36800-40611 2) Sprouts Farmers Market, Organic Salted Microwave
    Category
    Food
    Distribution
    21 states
  • SevereFDA (Drugs)·D-1623-2020·2020-09-30

    Preferred Pharmaceuticals Recalls Nature-Throid Tablets Due to CGMP Deviations

    Preferred Pharmaceuticals is voluntarily recalling specific lots of Nature-Throid tablets due to Current Good Manufacturing Practice (CGMP) deviations. The affected repackaged tablets were sold to three physicians in California and Georgia.

    Product
    Nature-Throid, 1 Grain, 65 mg (Thyroid U.S.P. 1 gr. (65mg)/Liothyronine (T3) 9mcg/Levothyroxine (T4) 38mcg, packaged in a) 90-count bottles (NDC 68788-7604-09), b) 100-count tablets (NDC 68788-7604-01), Rx Only, Mfg: RLC Labs; Cave Creek, AZ, Preferred Pharmaceuticals, Inc.
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2941-2020·2020-09-30

    MicroPort Recalls PROFEMUR Titanium Hip Prosthesis Components Due to Fracture Reports

    MicroPort Orthopedics is recalling specific PROFEMUR Titanium hip prosthesis components due to reports of fractures after implantation.

    Product
    PROFEMUR Neck Long Titanium, Catalog Numbers: PHA01204, PHA01214, PHA01224, PHA01234, PHA01244, PHA01254, PHA01264. Hip prosthesis component.
    Category
    Medical Device
    Distribution
    0 states
  • SevereCPSC·20193·2020-09-30

    STIHL Recalls Mini-Cultivator Attachments Due to Laceration Hazard

    STIHL is recalling about 185,000 mini-cultivator attachments because the gearbox may be installed upside down, causing tines to rotate toward the operator and posing a laceration risk.

    Product
    STIHL BF-KM Mini-Cultivator attachments
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1529-2020·2020-09-30

    Frito-Lay Classic Cube Mix Recalled for Undeclared Milk

    Frito-Lay is recalling 28-count Classic Cube Mix boxes because they may contain undeclared milk. The product was distributed to retail and foodservice channels in 11 western states.

    Product
    Frito-Lay 28 count Classic Cube Mix cube box UPC 28400 15586 1 oz. individual bags packaged in a larger non-flexible box
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Drugs)·D-1593-2020·2020-09-30

    Zanilast+ Gel Antiseptic Hand Sanitizer Recalled for Potential 1-Propanol Contamination

    Nanomateriales S.A. de C.V. is recalling 1,000 kg of Zanilast+ Gel Antiseptic Hand Sanitizer due to GMP deviations that may result in the presence of 1-propanol.

    Product
    Zanilast+ Gel Antiseptic Hand Sanitizer (70% Ethyl Alcohol) Packaged in 25 kg bottles, Distributed by Fujimura Trading S.A. DE C.V. Juventino Rosas 1902, Col. Caracol, 64810, Monterrey, N.L., Mexico Nanomateriales S.A. DE C.V. NDC 69912-006-01
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-1586-2020·2020-09-30

    Leafree Hand Sanitizer Recalled for Lacking FDA Approval

    Corgiomed LLC is recalling Leafree Instant Hand Sanitizer because it was marketed without FDA approval and labeled as edible alcohol.

    Product
    Leafree Instant Hand Sanitizer Aloe Vera (ethyl alcohol 70% v/v), Kills 99.99% Germs, EDIBLE ALCOHOL, a) 100 mL bottles, UPC code 6970495860325, b) 300 mL bottles, UPC code 6970495860318, and c) 500 mL bottles, UPC code 6970495860301, Exclusively Distributed by: Corgiomed LLC, Mc
    Category
    Drug
    Distribution
    2 states