The Recall Desk

State

Michigan product recalls

72,820 recalls have nationwide distribution and so reach Michigan. 9,516 additional recalls listed Michigan specifically in their distribution scope.

What the numbers show

Total
9,516
Critical
1,556
Severe
2,143
Most recent
2026-09-02

Of the 9,516 recalls naming Michigan we have scored against our rubric, 1,556 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,143 (23%) are Severe.

These figures cover only the 9,516 recalls whose distribution notice names Michigan specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

601–625 of 82336

  • ModerateFDA (Drugs)·D-0736-2026·2026-07-29

    Drug Recall: Dabigatran Etexilate Capsules 150 mg by Ascend Laboratories

    Ascend Laboratories is recalling 2,717 cartons of Dabigatran Etexilate Capsules, 150 mg, because stability testing found impurities above specification.

    Product
    DABIGATRAN ETEXILATE — DABIGATRAN ETEXILATE (DABIGATRAN ETEXILATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0724-2026·2026-07-29

    Cyproheptadine Hydrochloride Syrup Recall Due to Precipitate

    Rising Pharma is recalling cyproheptadine hydrochloride syrup due to the presence of precipitate, including crystallization and floating particles in the bottle.

    Product
    CYPROHEPTADINE HYDROCHLORIDE — CYPROHEPTADINE HYDROCHLORIDE (CYPROHEPTADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2775-2026·2026-07-29

    SnapshotGLO Wound Imaging Device Recalled Due to Battery Charging Software Issue

    Kent Imaging, Inc. is recalling SnapshotGLO Wound Imaging Devices (Models KB100 and KB100AA) because software issues may prevent the device from recharging.

    Product
    SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2761-2026·2026-07-29

    Olympus 4K UHD LCD Monitors Recalled Due to Potential Connector Faults

    Olympus Corporation of the Americas is recalling 10 Olympus 4K UHD LCD Monitors (Model OEV321UH) because the HDMI and DisplayPort connectors may become faulty.

    Product
    Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual display unit designed for displaying graphical information in color.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2758-2026·2026-07-29

    Phantom Hindfoot Guide Rods Recalled Due to Sterile Barrier Breaches

    Paragon 28 is recalling specific Phantom Hindfoot TTC/TC Ball Tipped Guide Rods because of complaints regarding breaches in the sterile pouch packaging.

    Product
    P28 PHANTON INTRAMEDULLARY NAIL SYSTEM, Phantom Hindfoot TTC/TC Ball Tipped Guide Rod, SIZE: 0.30 mm, LENGTH: 800 mmm, ITem number P31-955-1800-S; provides stabilization of the hindfoot and ankle.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2773-2026·2026-07-29

    Pipeline Flex Embolization Devices Recalled Due to Incorrect Labeling of Implant Length

    Micro Therapeutics, Inc. is recalling Pipeline Flex Embolization Devices because the labeled implant length does not match the actual device length.

    Product
    Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 12 mm 027 REF PED2-300-12. Intracranial aneurysm flow diverter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·PHA-07292026-01·2026-07-29

    Red's Steak Cilantro Lime Burrito misbranded with undeclared egg allergen

    USDA FSIS issued a public health alert for Red's All Natural steak burritos that contain undeclared egg and were incorrectly labeled. The product was distributed to Costco locations in Illinois, Michigan, and Minnesota.

    Product
    RED'S ALL NATURAL, LLC. — FSIS Issues Public Health Alert for Steak Burrito Product Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2763-2026·2026-07-29

    Halyard EYE PACK Convenience Kits Recalled Due to Incorrect Betadine Concentration

    AVID Medical, Inc. is recalling certain Halyard EYE PACK convenience kits because the Betadine solution contained within them has an incorrect concentration.

    Product
    Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2769-2026·2026-07-29

    Silent Nite Sleep Appliance Recalled Due to Lack of FDA Clearance

    Prismatik Dentalcraft, Inc. is recalling Silent Nite Sleep Appliances because the device does not have FDA clearance.

    Product
    Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Catalog Number: SILNT Product Description: Silent Nite Sleep Appliance is a mandibular advancement device (MAD) intended to treat snoring and mild to moderate obstructive sleep apnea (OSA).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0712-2026·2026-07-29

    FDA Recalls Amlodipine and Olmesartan Tablets Over Failed Dissolution Test

    Ascend Laboratories is recalling 6,192 bottles of Amlodipine and Olmesartan Medoxomil tablets nationwide due to failed dissolution specifications and Olmesartan content below specifications.

    Product
    AMLODIPINE AND OLMESARTAN MEDOXOMIL — AMLODIPINE AND OLMESARTAN MEDOXOMIL (AMLODIPINE AND OLMESARTAN MEDOXOMIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0758-2026·2026-07-29

    Supernus Recalls Trokendi XR Capsules for Failed Dissolution Specifications

    Supernus Pharmaceuticals is recalling Trokendi XR (topiramate) capsules because they failed dissolution specifications. The recall covers 15,853 bottles distributed nationwide.

    Product
    TROKENDI XR — TROKENDI XR (TOPIRAMATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V488000·2026-07-28

    Newell Recalls 2025-2027 P50 Coaches Due to Air Spring Defect

    Newell Coach Corp. is recalling 2025-2027 P50 coaches because the steer axle air spring base may crack, potentially causing loss of suspension support and increasing crash risk.

    Product
    NEWELL — NEWELL P50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V487000·2026-07-28

    Ford Recalls 2023-2025 Mustang Mach E for Rear Window Trim Defect

    Ford is recalling 2023-2025 Mustang Mach E vehicles because rear side quarter window glass trim may detach, creating a road hazard and increasing crash risk.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V484000·2026-07-27

    Jayco Recalls 2024-2026 Entegra Motorhomes Due to Brake Light Defect

    Jayco is recalling certain 2024-2026 Entegra motorhomes because exterior brake lights may stay on when brakes are not applied, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA REATTA XL, CORNERSTONE RESERVE, REATTA, ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V486000·2026-07-27

    Foretravel Recalls Realm Motorcoaches Due to Brake Light Defect

    Foretravel is recalling 2025-2027 Realm and Realm Presidential motorcoaches because exterior brake lights may stay on, increasing crash risk.

    Product
    FORETRAVEL — FORETRAVEL REALM PRESIDENTIAL, REALM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V483000·2026-07-27

    Jayco Recalls 2026 Entegra Anthem Motorhomes for Incorrect Tire Label

    Jayco is recalling 2026 Entegra Anthem motorhomes because the vehicle certification label may list the wrong tire size, which could lead to installing incorrect replacement tires.

    Product
    ENTEGRA — ENTEGRA ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V481000·2026-07-24

    Mercedes-Benz Recalls Various Models Due to Driver's Door Lock Defect

    Mercedes-Benz USA, LLC is recalling certain 2020-2026 Mercedes-Benz vehicles because a faulty door lock micro-switch may cause the vehicle to roll away.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLA 35, AMG GLB35 4MATIC, AMG GLC43 4MATIC, GLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide