The Recall Desk

State

Michigan product recalls

73,218 recalls have nationwide distribution and so reach Michigan. 9,548 additional recalls listed Michigan specifically in their distribution scope.

What the numbers show

Total
9,548
Critical
1,566
Severe
2,158
Most recent
2026-09-25

Of the 9,548 recalls naming Michigan we have scored against our rubric, 1,566 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,158 (23%) are Severe.

These figures cover only the 9,548 recalls whose distribution notice names Michigan specifically. The 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13151–13175 of 82766

  • HighCPSC·24161·2024-03-14

    U.S. Boiler Company Recalls Gas-Fired Residential Boilers for Carbon Monoxide Hazard

    About 2,500 U.S. Boiler, New Yorker Boiler, Advantage, FORCE, and Archer brand gas-fired boilers are recalled because the blocked vent switch can fail at altitudes above 5,400 feet, allowing carbon monoxide to accumulate in homes. No injuries have been reported.

    Product
    U.S. Boiler, New Yorker Boiler, Advantage, FORCE and Archer brand gas-fired hot water residential boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24159·2024-03-14

    Insignia Air Fryers and Ovens Recalled for Fire and Burn Hazards

    Best Buy is recalling about 187,400 Insignia brand air fryers and air fryer ovens sold from November 2021 through November 2023 because the units can overheat, causing handles to melt, glass doors to shatter, and fires.

    Product
    Air Fryers and Air Fryer Ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24160·2024-03-14

    Tracker Off Road OX EV Light Utility Vehicles Recalled for Fire Hazard

    About 500 Tracker Off Road OX EV vehicles are being recalled due to water entering the lithium-ion battery pack, which can cause a fire. No injuries have been reported.

    Product
    Tracker Off Road OX EV Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1035-2024·2024-03-13

    Frios Gourmet Pops Frozen Popsicles Recalled for Undeclared Egg Allergen

    Frios Gourmet Pops frozen popsicles are being recalled because they contain undeclared egg, an allergen. Consumers with egg allergies may face allergic reactions if they consume these products.

    Product
    Frios Gourmet Pops - Banana Pudding Popsicle 3oz frozen popsicle packaged individually in clear plastic sleeve. 48 popsicles per box. *Sold directly to end consumer via food truck
    Category
    Food
    Distribution
    17 states
  • CriticalFDA (Food)·F-1044-2024·2024-03-13

    Vegetarian Pia Cake Taro Durian Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling Vegetarian Pia Cake Taro Durian (14 oz bags) due to undeclared egg allergen. The recall affects approximately 222,320 bags distributed across 31 U.S. states and Canada.

    Product
    Vegetarian Pia Cake Taro Durian, 14 oz (400g)
    Category
    Food
    Distribution
    32 states
  • CriticalFDA (Food)·F-1050-2024·2024-03-13

    Vegetarian Pia Cake Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling 222,320 bags of Vegetarian Pia Cake Mung Bean Pineapple for containing undeclared egg. The product was distributed across 31 U.S. states and Canada.

    Product
    Vegetarian Pia Cake Mung Bean Pineapple, 14oz (400g)
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1049-2024·2024-03-13

    Vegetarian Pia Cake Recalled Due to Undeclared Egg Allergen

    LQNN Inc. is recalling Vegetarian Pia Cake Mungbean Durian (14oz) distributed across 31 U.S. states and Canada due to undeclared egg allergen, which poses serious risk to consumers with egg allergies.

    Product
    Vegetarian Pia Cake Mungbean Durian, 14oz (400g)
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1043-2024·2024-03-13

    Vegetarian Pia Cake Mung Bean Pumpkin Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling 222,320 bags of Vegetarian Pia Cake Mung Bean Pumpkin because the product contains undeclared egg allergen. Consumers with egg allergies should not eat this product.

    Product
    Vegetarian Pia Cake Mung Bean Pumpkin, 14 oz (400g)
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-1186-2024·2024-03-13

    MIC Gastric-Jejunal Feeding Tube Kits Recalled Over Defective Syringe

    Avanos Medical is recalling MIC Gastric-Jejunal Feeding Tube Kits because they contain a sterile pre-filled syringe that was subsequently recalled by Nurse Assist. Approximately 10,808 units have been distributed worldwide.

    Product
    MIC* Gastric-Jejunal Feeding Tube with ENFit Connectors: a) MIC* Gastric-Jejunal Feeding Tube Kit with ENFit Connector - Endoscopic/Radiologic Placement - 16 Fr, Product Code 8250-16; b) MIC* Gastric-Jejunal Feeding Tube Kit with ENFit Connector - Endoscopic/Radiologic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1042-2024·2024-03-13

    BANH PIA Hopia Cake Recalled Due to Undeclared Egg Allergen

    LQNN Inc. is recalling BANH PIA Hopia Cake due to undeclared egg allergen. Approximately 222,320 bags were distributed to 31 U.S. states and Canada.

    Product
    BANH PIA Hopia Cake, Mung Bean - Durian, 16.8 oz (480g)
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1046-2024·2024-03-13

    Vegetarian Pia Cake Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling approximately 222,320 bags of Vegetarian Pia Cake Black Sesame Durian due to undeclared egg. Consumers with egg allergies should not consume this product.

    Product
    Vegetarian Pia Cake Black Sesame Durian, 14oz (400g)
    Category
    Food
    Distribution
    32 states
  • SevereNHTSA·24V195000·2024-03-13

    Cushman Hauler Pro LSV Recalled for Battery Fire Risk

    Textron is recalling 2024 Cushman Hauler Pro LSV vehicles because a dump bed latch may crack or puncture the battery case, increasing the risk of a fire.

    Product
    CUSHMAN — CUSHMAN HAULER PRO LSV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1048-2024·2024-03-13

    BANH PIA Hopia Cake Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling BANH PIA Hopia Cake Mungbean Durian due to undeclared egg allergen. The product was distributed to customers in 31 U.S. states and Canada.

    Product
    BANH PIA Hopia Cake Mungbean Durian, 9.7oz (275g)
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1051-2024·2024-03-13

    Vegetarian Pia Cake Pandan Durian Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling 222,320 bags of Vegetarian Pia Cake Pandan Durian due to undeclared egg allergen. Consumers with egg allergies should not consume this product.

    Product
    Vegetarian Pia Cake Pandan Durian, 14oz (400g)
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1024-2024·2024-03-13

    Golden Owl Dried Mango Recall for Undeclared Sulfites

    Golden Owl Dried Mango (7 oz) is recalled due to undeclared sulfites. Consumers with sulfite sensitivity should not consume this product.

    Product
    Golden Owl Dried Mango 7 oz (200g) UPC 816710-024461. Packaged in clear non-flex plastic jars. 24 jars per case.
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-1053-2024·2024-03-13

    BANH PIA Pumpkin Pia Cake Recalled for Undeclared Egg Allergen

    BANH PIA Liu Sha Pumpkin Pia Cake is recalled because it contains egg that is not declared on the label. The recall affects 222,320 bags distributed across 31 US states and Canada. Consumers with egg allergies should not consume this product.

    Product
    BANH PIA Liu Sha Pumpkin Pia Cake, 480g
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1047-2024·2024-03-13

    FDA recalls Banh Pia Classic Hopia for undeclared egg allergen

    LQNN Inc. is recalling Banh Pia Classic Hopia because it contains undeclared egg allergen, which can cause serious allergic reactions. About 222,320 bags were distributed across 31 U.S. states and Canada.

    Product
    Banh Pia Classic Hopia, Mung Bean Durian, 16.8oz (480g)
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1052-2024·2024-03-13

    Vegetarian Pia Cake Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling Vegetarian Pia Cake Red Bean Durian products due to undeclared egg allergen. The recall affects 222,320 bags distributed across 31 U.S. states and Canada.

    Product
    Vegetarian Pia Cake Red Bean Durian, 14oz (400g)
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-1187-2024·2024-03-13

    Avanos Medical recalls MIC gastric-jejunal feeding tubes with defective syringe

    Avanos Medical is recalling MIC Gastric-Jejunal Feeding Tube Kits containing a sterile pre-filled syringe that was recalled by Nurse Assist. Approximately 53,126 units were distributed worldwide.

    Product
    MIC* Gastric-Jejunal Feeding Tube, Endoscopic/Radiologic Placement, GJ-Tube: a) MIC* Gastric-Jejunal Feeding Tube Kit - Endoscopic/Radiologic Placement - 16 Fr, Product Code 0250-16; b) MIC* Gastric-Jejunal Feeding Tube Kit - Endoscopic/Radiologic Placement - 16 Fr, Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1276-2024·2024-03-13

    ConvaTec Natura Stomahesive surgical ostomy system pouch-flange coupling mismatch

    ConvaTec Natura Stomahesive ostomy kits contain a 45mm flange but 57mm pouch, creating an incompatible coupling. The mismatch prevents the components from fitting together properly.

    Product
    ConvaTec Natura Stomahesive Post-Operative / Surgical Ostomy System, REF 416938, 1 3/4 in. 45mm, Sterile.
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Devices)·Z-1263-2024·2024-03-13

    Orthopedic knee implant recalled for potential sterile packaging breaches

    Howmedica Osteonics Corp. is recalling the NO 3 Triathlon TS Plus Tibial Insert due to potential breaches in the sterile packaging. The breaches could compromise product sterility and safety.

    Product
    NO 3 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1225-2024·2024-03-13

    Laboratory analyzer software defect may cause erroneous patient test results

    A software defect in VITROS 4600 Chemistry Systems causes quality control baselines to not update when users change them, potentially causing erroneous patient results.

    Product
    VITROS 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440 (refurbished)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1232-2024·2024-03-13

    Laboratory chemistry system software defect impairs quality control reporting

    A software defect in VITROS XT 3400 Chemistry Systems prevents quality control rules from properly reporting failures in test controls. This may result in erroneous patient test results being reported.

    Product
    VITROS XT 3400 Chemistry System, Catalog No. 6844458
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1230-2024·2024-03-13

    VITROS 4600 Chemistry System Software Defect Affects Quality Control Reporting

    A software defect in VITROS 4600 Chemistry Systems running software versions 3.8.0 or 3.8.1 prevents quality control rules from being flagged or reported correctly, potentially allowing erroneous patient results to be released.

    Product
    VITROS 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440 (refurbished)
    Category
    Medical Device
    Distribution
    Distributed nationwide