The Recall Desk

State

Michigan product recalls

20,199 recalls have nationwide distribution and so reach Michigan. 0 additional recalls listed Michigan specifically in their distribution scope.

About recalls in Michigan

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Michigan consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

10976–11000 of 20199

  • SevereCPSC·24722·2023-11-30

    Polaris Model Year 2022 Patriot 850 MATRYX Snowmobiles Recalled for Injury Hazard

    Polaris is recalling about 2,900 Model Year 2022 Patriot 850 MATRYX snowmobiles because the ring gear on the primary clutch can fail, causing clutch components to come loose and creating an injury hazard. Nine failures have been reported, including one injury.

    Product
    Polaris Snowmobiles, Model Year 2022 PATRIOT 850 MATRYX RMK, INDY and SWITCHBACK
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24725·2023-11-30

    Klickpick Home Children's Cup Sets Recalled for Lead and Choking Hazards

    Klickpick Home is recalling about 3,600 stainless steel children's cup sets sold on Amazon from March through September 2023. The cups contain lead-bearing solder that exceeds federal limits, and the lids can crack and produce sharp edges and small parts.

    Product
    Klickpick Home Children's Cup Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24723·2023-11-30

    Pack and Play Mattresses Recalled for Infant Suffocation Hazard

    DODO Baby House pack and play mattresses sold on Amazon violate federal crib mattress safety standards and pose a suffocation hazard to infants. Consumers should stop using the mattresses immediately and destroy them.

    Product
    DODO Baby House Pack and Play Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24033·2023-11-30

    GE JP3030 Electric Cooktops Recalled for Burn Hazard Risk

    GE Appliances is recalling about 11,000 JP3030 knob-control electric radiant cooktops because burners can remain on after being turned to the "off" position due to misaligned or fractured knob components, posing a burn hazard. No injuries have been reported.

    Product
    Knob-control electric radiant cooktops, model GE JP3030
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24721·2023-11-30

    Vibe Bear Playyard Mattresses Recalled for Suffocation Hazard

    Beyond Baby Vibe Bear-branded playyard mattresses sold on Amazon.com from January to June 2023 are recalled due to suffocation hazards for infants. The mattresses violate federal crib mattress safety standards for firmness, thickness, warnings, and labels.

    Product
    Vibe Bear Playyard Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24720·2023-11-30

    Polaris Model Year 2023 Snowmobiles Recalled for Clutch Failure Injury Hazard

    Polaris is recalling about 2,200 Model Year 2023 PATRIOT 9R MATRYX PRO RMK and PATRIOT 9R MATRYX RMK KHAOS snowmobiles because the primary clutch can fail and cause clutch components to come loose, posing an injury hazard.

    Product
    Model Year 2023 PATRIOT 9R MATRYX PRO RMK and PATRIOT 9R MATRYX RMK KHAOS Snowmobiles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24034·2023-11-30

    Berkshire Heated Throws and Blankets Recalled for Fire and Burn Hazards

    Berkshire Blanket & Home Co. is recalling about 29,840 heated throws and blankets because they may overheat, posing fire and thermal burn hazards. The firm has received nine reports of the products burning, melting, or overheating, with no injuries reported.

    Product
    Heated Throws and Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24724·2023-11-30

    Tiblue Children's Cups Recalled for Lead Content and Lid Hazards

    Tiblue 8 oz and 12 oz stainless steel children's cups are being recalled because they contain lead in solder on the bottom exterior that exceeds federal limits, and the lids can crack and break during use, creating sharp edges and choking hazards.

    Product
    Tiblue 8 oz and 12 oz children's cups
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24032·2023-11-30

    Russound AW70V6 Loudspeakers Recalled for Impact Injury Hazard

    Russound is recalling Model AW70V6 loudspeakers because the front baffle can separate from the rear housing, causing the speaker to fall from its mounted location and create an impact injury hazard. One incident has been reported with no injuries.

    Product
    Russound Loudspeakers Model AW70V6
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24718·2023-11-30

    Supacaz Orbitron Bicycle Pedals Recalled for Fall Hazard

    Specialized Bicycle Components is recalling about 3,000 Supacaz Orbitron pedals because the pedal body can detach from the spindle or the spindle can break, posing a fall hazard. The company has received 21 reports of pedals breaking but no injuries have been reported.

    Product
    Supacaz Orbitron Pedals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0131-2024·2023-11-29

    Eye Drops Recalled for Non-Sterility Issues from Manufacturing Facility

    Cardinal Health is recalling LEADER brand Eye Irritation Relief drops due to non-sterility concerns. FDA testing found insanitary conditions and positive bacterial results at the manufacturing facility, affecting 11,629 units distributed nationwide.

    Product
    EYES IRRITATION RELIEF — EYES IRRITATION RELIEF (POLYVINYL ALCOHOL AND POVIDONE AND TETRAHYDROZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0107-2024·2023-11-29

    Polyvinyl Alcohol Eye Drops Recalled for Non-Sterile Manufacturing Conditions

    FDA recalls Polyvinyl Alcohol 1.4% Lubricating Eye Drops nationwide due to non-sterile manufacturing conditions found during inspection.

    Product
    Polyvinyl Alcohol 1.4% Lubricating Eye Drops, packaged in 0.5 FL OZ (15mL) bottles, Dist. by: RUGBY LABORATORIES, Livonia, MI 48152, NDC 0536-1325-94.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0234-2024·2023-11-29

    VariSoft Insulin Infusion Set Recalled Over Premature Connector Disconnection

    Unomedical recalls 3,362 units of VariSoft infusion sets due to connector damage causing premature disconnection and missed insulin doses, risking dangerous elevation of blood glucose and ketone levels.

    Product
    VariSoft infusion set, Model Number 1002830
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0132-2024·2023-11-29

    FDA Recalls Non-Sterile Dry Eye Relief Drops Due to Bacterial Contamination

    Cardinal Health is recalling all lots of LEADER brand Dry Eye Relief nationwide due to non-sterility. FDA found insanitary manufacturing conditions and positive bacterial test results.

    Product
    DRY EYE RELIEF — DRY EYE RELIEF (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0232-2024·2023-11-29

    VariSoft Infusion Set recalled for defective connector prone to unintended disconnection

    Unomedical is recalling 8,028 VariSoft infusion sets due to a manufacturing defect that makes the connector prone to unintended disconnection, potentially leading to missed insulin doses and serious blood glucose complications.

    Product
    VariSoft infusion set, Model Number 1002827
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0108-2024·2023-11-29

    Lubricating Tears Eye Drops Recalled for Non-Sterility and Bacterial Contamination

    Rugby Laboratories' Lubricating Tears Eye Drops are being recalled nationwide due to non-sterility. FDA found insanitary conditions and positive bacterial test results at the manufacturing facility.

    Product
    Lubricating Tears Eye Drops (Dextran/Hypromellose), 0.1%/0.3%, packaged in 0.5 FL OZ (15mL) bottles, Distributed by: RUGBY LABORATORIES, Livonia, MI 48152, NDC 0536-1282-94
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0134-2024·2023-11-29

    FDA Recalls LEADER Brand Lubricant Eye Drops Due to Non-Sterility Risk

    Cardinal Health is recalling all lots of LEADER brand Lubricant Eye Drops nationwide due to non-sterility. FDA found insanitary conditions and positive bacterial test results from the manufacturing facility.

    Product
    LUBRICANT DROPS — LUBRICANT DROPS (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0116-2024·2023-11-29

    FDA Recalls Sodium Bicarbonate Injection for Silicone Particulate Contamination

    Exela Pharma Sciences recalls 8.4% sodium bicarbonate injection nationwide due to silicone particulate matter in vials. The FDA classified this Class I recall as affecting 355,220 vials.

    Product
    SODIUM BICARBONATE — SODIUM BICARBONATE (SODIUM BICARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0136-2024·2023-11-29

    LEADER Lubricant Eye Drops Recalled for Non-Sterility and Bacterial Contamination

    Cardinal Health is recalling all lots of LEADER brand Lubricant Eye Drops due to non-sterility issues. FDA found insanitary conditions and positive bacterial test results at the manufacturing facility in India.

    Product
    LEADER brand Lubricant Eye Drops (Propylene Glycol, 0.6%); 0.33 FL OZ (10 mL) dropper bottles, Sterile, Distributed By Cardinal Health, Dublin, Ohio 43017. Made in India NDC: 70000-0587-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0117-2024·2023-11-29

    Midazolam Injectable Recalled for Silicone Particulate Matter Contamination

    Exela Pharma Sciences is recalling Midazolam Injectable due to silicone particulate matter contamination. Patients and healthcare providers with the affected lot should discontinue use and consult their healthcare provider.

    Product
    Midazolam in 0.8% Sodium Chloride Injection 100 mg/100 mL (1mg/mL), 100 mL Single-Dose Vial, 25 count carton, Ready to Use For Intravenous Infusion Only Preservative Free, Rx Only, Manufactured and Distributed by Exela Pharma Sciences, LLC, Lenoir, NC 28645, (Vial NDC 51754-2131-
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0135-2024·2023-11-29

    Eye drops recalled for non-sterility due to bacterial contamination

    Cardinal Health's LEADER brand Dry Eye Relief eye drops are recalled nationwide due to non-sterility concerns. FDA found insanitary conditions and positive bacterial results from environmental sampling at the manufacturing facility.

    Product
    DRY EYE RELIEF — DRY EYE RELIEF (POLYETHYLENE GLYCOL AND PROPYLENE GLYCOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0233-2024·2023-11-29

    VariSoft Infusion Set Model 1002828 Recalled for Connector Detachment Risk

    The FDA recalls 1,679 VariSoft infusion sets (Model 1002828) due to connector damage that causes improper detachment. Undetected disconnections can lead to missed insulin doses and diabetic ketoacidosis.

    Product
    VariSoft infusion set, Model Number 1002828
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0133-2024·2023-11-29

    LEADER Lubricant Eye Drops Recalled Nationwide for Non-Sterility Concerns

    LEADER brand Lubricant Eye Drops are being recalled nationwide due to non-sterility issues. FDA testing found insanitary conditions and positive bacterial contamination at the manufacturing facility.

    Product
    LUBRICANT DROPS — LUBRICANT DROPS (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0113-2024·2023-11-29

    Buspirone Hydrochloride Tablets Recalled Due To Amlodipine Contamination Risk

    FDA recalls Buspirone Hydrochloride 10 mg tablets due to potential contamination with foreign Amlodipine Besylate tablets. The recall affects 1,344 blister cards distributed nationwide.

    Product
    BUSPIRONE HYDROCHLORIDE — BUSPIRONE HYDROCHLORIDE (BUSPIRONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide