The Recall Desk

State

Colorado product recalls

73,187 recalls have nationwide distribution and so reach Colorado. 6,945 additional recalls listed Colorado specifically in their distribution scope.

What the numbers show

Total
6,945
Critical
1,218
Severe
1,510
Most recent
2026-10-02

Of the 6,945 recalls naming Colorado we have scored against our rubric, 1,218 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,510 (22%) are Severe.

These figures cover only the 6,945 recalls whose distribution notice names Colorado specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11676–11700 of 80132

  • SevereFDA (Food)·F-1336-2024·2024-06-12

    Danisco Yogurt Stabilizer System Recalled for Potential Salmonella

    Danisco USA Inc. is recalling Yogurt 6626 Stabilizer System due to potential Salmonella contamination. The product was distributed across 23 US states, Canada, and Mexico.

    Product
    Yogurt 6626 Stabilizer System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereNHTSA·24V433000·2024-06-12

    2025 Kenworth and Peterbilt Trucks Steering Linkage Defect

    PACCAR is recalling 2025 Kenworth and Peterbilt trucks due to improperly heat-treated ball studs in steering assemblies that may break, causing loss of steering control.

    Product
    KENWORTH — KENWORTH, PETERBILT T880, T480, T380, T280
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V429000·2024-06-12

    Forest River Recalls School Buses Due to Insufficient Crash Protection

    Forest River is recalling 3,192 school buses because the restraining barrier may not provide sufficient protection in a crash, increasing injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, FOREST RIVER BUS QUEST, QUEST XL, STARCRAFT ALLSTAR MPV, STARCRAFT ALLSTAR XL MVP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1306-2024·2024-06-12

    Danisco Food Additive Recalled for Potential Salmonella Contamination

    Danisco USA Inc. is recalling Grindsted Whipped Cream #2 stabilizer system due to potential Salmonella contamination. The product was distributed in 24 US states, Canada, and Mexico.

    Product
    Grindsted Whipped Cream #2 rBST-fr, Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Devices)·Z-1877-2024·2024-06-12

    Sevoflurane Vaporizer Component Recall Due to Hydrogen Fluoride Degradation

    Getinge's sevoflurane vaporizer component may degrade into hydrogen fluoride, posing inhalation and skin exposure risks to healthcare workers and patients. The FDA Class I recall affects 120 units distributed across six U.S. states.

    Product
    Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20, Flow-i C30,Flow-i C40, Flow-c, Flow-e.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Food)·F-1316-2024·2024-06-12

    Grindsted Creamer 2103 Stabilizer System Recalled for Potential Salmonella

    Danisco USA Inc. is recalling Grindsted Creamer 2103 Stabilizer and Emulsifier System due to potential Salmonella contamination. Approximately 36,265 kg was distributed across multiple U.S. states, Canada, and Mexico.

    Product
    Grindsted Creamer 2103 Stabilizer and Emulsifier System, 22. 68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1311-2024·2024-06-12

    Sweetener Blend Recalled for Potential Salmonella Contamination

    Danisco USA Inc. is recalling Reese SG FR Sweetener Blend, CM50 due to potential Salmonella contamination. The recall affects product distributed across 24 US states, Canada, and Mexico.

    Product
    Reese, SG FR Sweetener Blend, CM50
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1325-2024·2024-06-12

    Food Additive Recalled for Potential Salmonella Contamination

    Danisco USA Inc. is recalling Grindsted GSD 1076 Stabilizer and Emulsifier System in 50-pound bags due to potential Salmonella contamination. The product was distributed to multiple US states, Canada, and Mexico.

    Product
    Grindsted GSD 1076 Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1335-2024·2024-06-12

    Sour Cream Stabilizer System Recalled for Potential Salmonella Contamination

    Danisco USA Inc. recalls Grindsted Sour Cream 6563 stabilizer system for potential Salmonella contamination affecting 33,600 kg distributed across the US, Canada, and Mexico.

    Product
    Grindsted Sour Cream 6563 non-GM Stabilizer System 20 kg/ 44.09 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1320-2024·2024-06-12

    Sweet roll dough blend recalled due to potential Salmonella contamination

    Danisco USA Inc. is recalling Grindsted Sweet Roll Dough Blend 2 Stabilizer & Emulsifier System due to potential Salmonella contamination. The product was distributed across the US, Canada, and Mexico.

    Product
    Grindsted Sweet Roll Dough Blend 2 Stabilizer & Emulsifier System 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1318-2024·2024-06-12

    Grindsted Creamer 2160 System Recalled for Salmonella Contamination

    Danisco USA Inc. is recalling Grindsted Creamer 2160 System bags due to potential Salmonella contamination. The recall affects 31,865.40 kg distributed across the US, Canada, and Mexico.

    Product
    Grindsted Creamer 2160 System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1327-2024·2024-06-12

    Avicel-plus Food Stabilizer Additive Recalled for Potential Salmonella

    Danisco USA Inc. is recalling Avicel-plus GP 1615 Stabilizer System FCC due to potential Salmonella contamination. The affected bulk food additive was distributed to manufacturers across multiple U.S. states, Canada, and Mexico.

    Product
    Avicel-plus GP 1615 Stabilizer System FCC, 1000 kg / 2204.62 bulk bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1305-2024·2024-06-12

    Danisco Germantown Stabilizer 1772-II Recalled for Salmonella

    Danisco USA Inc. is recalling Germantown Stabilizer 1772-II, a food stabilizer and emulsifier system, due to potential Salmonella contamination. The product was distributed across the U.S., Canada, and Mexico.

    Product
    Germantown Stabilizer 1772-II, Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1313-2024·2024-06-12

    Grindsted Stabilizer System Recalled for Potential Salmonella Contamination

    Danisco USA Inc. is recalling Grindsted CFF 1455 Stabilizer System due to potential Salmonella contamination. The product was distributed to commercial customers in 24 US states, Canada, and Mexico.

    Product
    Grindsted(R) CFF 1455 Stabilizer System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1317-2024·2024-06-12

    ASC 2138 Stabilizer and Emulsifier System Recalled for Salmonella

    Danisco USA Inc. recalls ASC 2138 Stabilizer and Emulsifier System due to potential Salmonella contamination. Affected product distributed across US, Canada, and Mexico.

    Product
    ASC 2138 Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1333-2024·2024-06-12

    Danisco Grindsted Sweetlife Cinnamon Roll Stabilizer Recalled for Salmonella

    Danisco USA Inc. is recalling Grindsted Sweetlife CINN. Roll BAS Stabilizer & Emulsifier System due to potential Salmonella contamination. The product was distributed across 28 U.S. states, Canada, and Mexico.

    Product
    Grindsted Sweetlife CINN. Roll BAS Stabilizer & Emulsifier System, 22.68 kg/ 50 lb bag
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-1960-2024·2024-06-12

    Vascular graft devices recalled due to slider component separation

    Atrium Medical is recalling ADVANTA VXT vascular grafts following complaints of separation between the slider component and swivel core.

    Product
    ADVANTA VXT, 7X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1969-2024·2024-06-12

    Vascular graft component separation: Atrium Medical ADVANTA VXT recall

    Atrium Medical is recalling ADVANTA VXT vascular grafts due to reported separation of the slider mechanism from the core component, which could compromise device integrity.

    Product
    ADVANTA VXT, 7X70, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1972-2024·2024-06-12

    Vascular Graft Component Separation Risk in ADVANTA VXT Models

    Atrium Medical Corporation recalled 53,308 ADVANTA VXT vascular grafts worldwide due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. Patients should consult their healthcare provider regarding appropriate follow-up care.

    Product
    ADVANTA VXT, 7X80, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1935-2024·2024-06-12

    LOSPA Patella Knee Component Recalled for Unsupported Expiration Date

    CORENTEC's LOSPA Patella Component knee implants are recalled due to an unsupported 10-year expiration date. Thirty-five units were distributed nationwide.

    Product
    LOSPA Patella Component Model/Catalog Number: 01.10.9XX Software Version: N/A Product Description: Patella
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1999-2024·2024-06-12

    Vascular Graft Swivel Rod Separation Reported in ADVANTA VXT Devices

    Atrium Medical recalls ADVANTA VXT vascular grafts due to reported separation of the slider swivel rod from its core, creating a gap between components. No injuries reported.

    Product
    ADVANTA VXT, 4-7X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1986-2024·2024-06-12

    Vascular graft component separation reported in Advanta VXT devices

    Atrium Medical Corporation recalls Advanta VXT vascular grafts due to separation of internal swivel components. Approximately 53,308 units worldwide are affected, with the slider GDS swivel rod potentially separating from its core.

    Product
    ADVANTA VXT, 6X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide