The Recall Desk

State

Missouri product recalls

73,817 recalls have nationwide distribution and so reach Missouri. 8,501 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,501
Critical
1,339
Severe
2,204
Most recent
2026-11-04

Of the 8,501 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,204 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43376–43400 of 82318

  • HighFDA (Devices)·Z-1410-2018·2018-04-25

    Philips CT Scanner Recall Due to Emergency Stop Defect

    Philips is recalling 106 Brilliance Big Bore CT scanners because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient loading or unloading.

    Product
    Brilliance Big Bore (Oncology) - Model no. 728243, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1030-2018·2018-04-25

    Festival Foods Potato Salad Recalled for Undeclared Imitation Crab Meat

    Mrs Gerry's Kitchen is recalling Festival Foods Potato Salad because it may contain undeclared traces of imitation crab meat.

    Product
    Festival Foods Potato Salad packaged in the following size containers: Net Wt. 6 oz. (170g), UPC 17839-22388, Net Wt. 1 lb. (454 g) UPC 17839-22301, Net Wt. 3 lb. (1.36 kg), UPC 17839-22303. Net Wt. 35 lb. 15.87 kg), UPC 17839-22335. Keep Refrigerated. Made for…
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-1402-2018·2018-04-25

    Siemens PRIMUS HI Digital Linear Accelerator Software Recall

    Siemens is recalling 18 PRIMUS HI Digital Linear Accelerators to update software and reduce the risk of collision during automated cancer treatments.

    Product
    PRIMUS HI, Digital Linear Accelerator, Model No. 04504200 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1431-2018·2018-04-25

    Philips Intera 0.5T MRI Recalled for Helium Gas Risk

    Philips is recalling 8,205 Intera 0.5T MRI scanners worldwide due to a potential risk of helium gas release during a magnet quench.

    Product
    Intera 0.5T Standard, Model 781101 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1406-2018·2018-04-25

    Philips Ingenuity Core CT Systems Recalled for Couch Movement Hazard

    Philips is recalling 281 Ingenuity Core CT systems because the emergency stop may fail to lock the couch, allowing it to move during patient loading.

    Product
    Ingenuity Core - Model no. 728321, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1381-2018·2018-04-25

    Zimmer Biomet Recalls Segmental System Proximal Femoral Components

    Zimmer Biomet is recalling specific proximal femoral components due to potential machining debris that may not have been adequately removed during cleaning.

    Product
    Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is used for solving complex salvage cases to address patients with severe bone loss associated with disease, trauma, or revision.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1081-2018·2018-04-25

    Midwest Northern Nut Lifetime Trail Mix Recalled for Allergen Cross-Contact

    Midwest Northern Inc. is recalling 35,056 lbs of Lifetime Trail Mix due to potential allergen cross-contact in the roasting oil.

    Product
    Midwest Northern Nut Lifetime Trail Mix. Net Wt. 25 lbs. Midwest Northern Inc., Minneapolis, MN 55118
    Category
    Food
    Distribution
    13 states
  • HighFDA (Devices)·Z-1397-2018·2018-04-25

    Siemens MEVATRON M2 Linear Accelerator Recalled for Collision Risk

    Siemens is recalling 18 MEVATRON M2 linear accelerators to update software and reduce the risk of collision during automated cancer treatments.

    Product
    MEVATRON M2 / PRIMUS Mid-Energy, Digital Linear Accelerator, Model No. 01940035 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1442-2018·2018-04-25

    Philips T5 MRI Scanner Recalled for Helium Gas Risk

    Philips is recalling T5 MRI scanners due to a potential risk of helium gas release during a magnet quench.

    Product
    T5 Model 78104 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1063-2018·2018-04-25

    Midwest Northern Nut Texas Twist Snack Mix Recalled for Allergen Cross-Contact

    Midwest Northern Inc. is recalling Texas Twist Snack Mix due to potential allergen cross-contact in the oil used to roast nuts and seeds.

    Product
    Midwest Northern Nut Texas Twist, Snack Mix. Packaged in the following sizes: 1. Net Wt. 16 oz. (454G), UPC 38043-90083. 2. Net Wt. 5 lbs. 3. Net Wt. 25 lbs. Midwest Northern Inc., Minneapolis, MN 55118
    Category
    Food
    Distribution
    13 states
  • HighFDA (Devices)·Z-1428-2018·2018-04-25

    Halyard Closed Suction System Flex Connectors May Disconnect During Use

    Halyard Health is recalling certain Closed Suction Systems because Flex Connectors may become loose or disconnect before or during use.

    Product
    Halyard Closed Suction System for Adults, Turbo- cleaning¿Closed¿Suction¿System¿for¿Adults,¿Double¿Swivel¿Elbow (DSE). Used to aspirate liquids or semisolids from a patient's upper airway. a. HALYARD* TURBO-CLEANING 14FR DSE 21.3IN/54 CM (GREEN); b. HALYARD* TRACH…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1083-2018·2018-04-25

    Midwest Northern Nut Oriental Mix Recalled for Potential Allergen Cross-Contact

    Midwest Northern Inc. is recalling Nut Oriental Mix snack mix due to potential allergen cross-contact in the oil used to roast nuts and seeds.

    Product
    Midwest Northern Nut Oriental Mix, Snack Mix. Packaged in the following sizes: 1. Net Wt. 5 lbs. 2. Net Wt. 10 lbs. 3. Net Wt. 15 lbs. Midwest Northern Inc., Minneapolis, MN 55118
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1075-2018·2018-04-25

    Midwest Northern Nut Cranberry Nut Trail Mix Recalled for Allergen Cross-Contact

    Midwest Northern Inc. is recalling 25 lb. bags of Cranberry Nut Trail Mix due to potential allergen cross-contact in the oil used to roast nuts and seeds.

    Product
    Midwest Northern Nut Cranberry Nut Trail Mix, Net Wt. 25 lbs. Midwest Northern Inc., Minneapolis, MN 55118
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1064-2018·2018-04-25

    Midwest Northern Trail Mix Recalled for Potential Allergen Cross-Contact

    Midwest Northern Inc. is recalling Midwest Trail Mix due to potential allergen cross-contact in the oil used to roast nuts and seeds.

    Product
    Midwest Northern Nut Midwest Trail Mix, Trail Mix. Net Wt. 16 oz. (454G), UPC 38043-90031. Midwest Northern Inc., Minneapolis, MN 55118
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1080-2018·2018-04-25

    Midwest Northern Nut Lake Elmo Mix Recalled for Allergen Cross-Contact

    Midwest Northern Inc. is recalling 35,056 lbs of Lake Elmo Mix due to potential allergen cross-contact in the roasting oil.

    Product
    Midwest Northern Nut Lake Elmo Mix. Net Wt. 25 lbs. Midwest Northern Inc., Minneapolis, MN 55118
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1082-2018·2018-04-25

    Midwest Northern Nut Mendakota Mix Recalled for Allergen Cross-Contact

    Midwest Northern Inc. is recalling Mendakota Mix due to potential allergen cross-contact in the oil used to roast the nuts and seeds.

    Product
    Midwest Northern Nut Mendakota Mix. Net Wt. 25 lbs. Midwest Northern Inc., Minneapolis, MN 55118
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1096-2018·2018-04-25

    Midwest Northern Nut Tropical Mix Recalled for Allergen Cross-Contact

    Midwest Northern Inc. is recalling Tropical Mix trail mix due to potential allergen cross-contact in the oil used to roast nuts and seeds.

    Product
    Midwest Northern Nut Tropical Mix, No Carob - No Coconut, Trail Mix. Packaged in the following sizes: 1. Net WT. 5 lbs. 2. Net Wt.25 lbs. Midwest Northern Inc., Minneapolis, MN 55118
    Category
    Food
    Distribution
    13 states
  • HighCPSC·18739·2018-04-25

    HD Supply Recalls Seasons Ceiling Fans Due to Impact Hazard

    HD Supply is recalling Seasons ceiling fans because brackets can break, causing blades to fall. No injuries have been reported, but one instance of minor property damage occurred.

    Product
    Seasons ceiling fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1400-2018·2018-04-25

    Siemens ONCOR Impression Linear Accelerator Software Update Recall

    Siemens is recalling seven ONCOR Impression Digital Linear Accelerators to update software and reduce the risk of collision during automated cancer treatments.

    Product
    ONCOR Impression , Digital Linear Accelerator, Model No. 05857920 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1058-2018·2018-04-25

    Midwest Northern Nut Nutty Fruit Mix Recalled for Allergen Cross-Contact

    Midwest Northern Inc. is recalling Nutty Fruit Mix and Trail Mix due to potential allergen cross-contact in the oil used to roast nuts and seeds.

    Product
    Midwest Northern Nut Nutty Fruit Mix, Trail Mix. Packaged in the following sizes: 1. Net Wt. 16 oz. (454G), UPC 38043-90027. 2, Net Wt. 25 lbs. Midwest Northern Inc., Minneapolis, MN 55118
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1037-2018·2018-04-25

    Midwest Northern Nut Redskin Peanuts Recalled for Potential Allergen Cross-Contact

    Midwest Northern Inc. is recalling Redskin Peanuts due to potential allergen cross-contact in the roasting oil. Consumers should stop using the product.

    Product
    Midwest Northern Nut Redskin Peanuts. Packaged in the following sizes: 1. Net Wt. 16 oz. (454G), UPC 38043-90112. 2. 2. Net Wt. 5 lbs. 3. Net Wt. 30 lbs. Midwest Northern Inc., Minneapolis, MN 55118
    Category
    Food
    Distribution
    13 states
  • HighFDA (Devices)·Z-1435-2018·2018-04-25

    Philips Achieva 1.5T MRI Systems Recalled for Helium Gas Risk

    Philips is recalling 8,205 Achieva 1.5T MRI systems worldwide due to a potential risk of helium gas release during a magnet quench.

    Product
    Achieva 1.5T: 1) Nova (Dual), Model 781173, 2) Achieva 1.5T Initial Systems Model 781178, 3) Achieva 1.5T Nova Model 781196, 4) Achieva 1.5T Conversion Model 781283, 5) Achieva 1.5T Model 781296, 6) Achieva 1.5T R5 based Model 781343, 7) Achieva 1.5T Conversion R5 based Model…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1074-2018·2018-04-25

    Midwest Northern Nut Franz Mix Recalled for Potential Allergen Cross-Contact

    Midwest Northern Inc. is recalling 35,056 lbs of Nut Franz Mix due to potential allergen cross-contact in the oil used to roast the nuts and seeds.

    Product
    Midwest Northern Nut Franz Mix, Nut Mix, Net Wt. 30 lbs. Midwest Northern Inc., Minneapolis, MN 55118
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1045-2018·2018-04-25

    Midwest Northern Nut Roasted Pecans Recalled for Allergen Cross-Contact

    Midwest Northern Inc. is recalling roasted and salted pecans due to potential allergen cross-contact in the roasting oil.

    Product
    Midwest Northern Nut Pecans Roasted & Salted. Packaged in the following sizes: 1. Net Wt. 16 oz. (454G), UPC 38043-90145. 2. Pecan Mammoth Halves, Roasted & Salted. Net Wt. 30 lbs. 3. Pecan Pieces Roasted & Salted Net Wt. 30 lbs. Midwest Northern Inc.…
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1050-2018·2018-04-25

    Midwest Northern Nut BBQ Blues Mix Recalled for Allergen Cross-Contact

    Midwest Northern Inc. is recalling its Nut BBQ Blues Mix due to potential allergen cross-contact in the oil used to roast the nuts and seeds.

    Product
    Midwest Northern Nut BBQ Blues Mix. Packaged in the following sizes: 1. Net Wt. 16 oz. (454G), UPC 38043-90084. 2. Net Wt. 5 lbs. Midwest Northern Inc., Minneapolis, MN 55118
    Category
    Food
    Distribution
    13 states