The Recall Desk

State

Michigan product recalls

20,308 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.

13426–13450 of 20308

  • HighNHTSA·22V344000·2023-05-05

    2022 Kia Telluride recall: instrument cluster display may go blank

    Excess adhesive in the instrument cluster circuit board may cause the display to go blank, preventing drivers from seeing critical information and increasing crash risk.

    Product
    KIA — 2022 KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V343000·2023-05-05

    2020-2023 Trailstar and Ranger Trail Boat Trailers Recalled for Hub Seizure

    Tracker Marine is recalling 2020-2023 Trailstar and Ranger Trail boat trailers because axle hubs were not tightened properly, which can cause hub seizure and loss of vehicle control.

    Product
    TRAILSTAR — 2021 TRAILSTAR BOAT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V327000·2023-05-05

    2023 Airstream Atlas Motorhomes Recalled for Electrical Fire Risk

    Airstream is recalling 2023 Atlas motorhomes due to undersized fuses that may allow wiring to overheat and increase fire risk. Dealers will replace the fuse and install a new circuit.

    Product
    AIRSTREAM — 2023 AIRSTREAM ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23751·2023-05-04

    Polaris Model Year 2022-2023 Snowmobiles Recalled for Fire Hazard

    Polaris is recalling about 14,885 Model Year 2022-2023 MATRYX RMK KHAOS and PRO snowmobiles. When the rider engages the throttle and brake simultaneously, the brake system can overheat, posing a fire hazard and risk of burn injuries.

    Product
    Model Year 2022-2023 MATRYX RMK KHAOS and PRO Snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23195·2023-05-04

    Ricky Powersports Youth ATVs recalled for safety standard violations

    About 570 Ricky Powersports youth ATVs fail to meet federal safety standards, including parking brake and labeling requirements. The defects pose a risk of serious injury or death.

    Product
    Ricky Powersports Youth All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23193·2023-05-04

    Walker Edison Twin Over Twin Bunk Beds Recalled for Fall Hazards

    Walker Edison Furniture is recalling about 121,000 Twin Over Twin Bunk Beds because the wooden slats supporting the beds can break while in use, posing fall and impact hazards. The company has received 14 incident reports, including one report of minor injuries.

    Product
    Twin Over Twin Bunk Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23754·2023-05-04

    Children's White Robes Recalled for Flammability Standards Violation

    The Company Store is recalling about 930 children's white robes sold online from September 2021 through November 2022 because they fail to meet federal flammability standards for children's sleepwear, posing a burn injury risk.

    Product
    Children's white robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23752·2023-05-04

    L.O.L. Surprise! Metal Doll Pins Recalled for Excessive Lead Paint

    Culture Fly is recalling approximately 6,600 L.O.L. Surprise! Trick or Treat subscription boxes sold with metal doll pins because the paint on the pins contains lead levels that exceed the federal lead paint ban, posing a lead poisoning hazard to young children.

    Product
    L.O.L. Surprise! Trick or Treat subscription boxes sold with Metal Doll Pins
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23753·2023-05-04

    Sahara Folding Food Dehydrators Recalled for Fire Hazard

    Berkshire Innovations is recalling about 990 Sahara Folding Food Dehydrators because the heater fan can fail and cause the unit to overheat, posing a fire hazard. No injuries or property damage have been reported.

    Product
    Sahara Folding Food Dehydrators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23196·2023-05-04

    Severe Weather Doorglass Inserts Recalled Due to Wind-Borne Debris Risk

    ODL Inc. is recalling Severe Weather Doorglass Inserts sold at Home Depot and Lowe's because the adhesive bond can separate during hurricanes, creating a risk of injury and property damage from windborne debris.

    Product
    Severe Weather Doorglass Inserts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0802-2023·2023-05-03

    Savor Imports IQF Raspberries recalled for potential Hepatitis A contamination

    Savor Imports IQF Whole Raspberries (Lot 20220210) are recalled nationwide due to potential Hepatitis A contamination. Consumers should not eat the product and should return or discard it.

    Product
    Savor Imports IQF Whole Raspberries; Net Wt 2-5lb; MFG# 341798; UPC: 10684476003771
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V166000·2023-05-03

    Newmar motorhomes recalled for loose steering column bolt

    Newmar is recalling 1,277 of its 2021 and 2022 motorhomes because the steering column bolt may not be properly tightened, potentially causing loss of steering control. Owners should contact dealers for free inspection and tightening.

    Product
    NEWMAR — 2021 NEWMAR NEW AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1438-2023·2023-05-03

    Surgical Kit Light Handle Covers May Separate During Use

    ROi CPS LLC is recalling 1,369 sterile surgical convenience kits because light handle covers may separate and fall off during use. The affected kits were distributed nationwide in Florida and Missouri.

    Product
    Sterile surgical convenience kits: 1. regard Item Number: 880473001, OR01105A - Total Shoulder/Hip; 2. regard Item Number: 880426004, OR01033D - Total Hip; 3. regard Item Number: 880427003, OR01034C - Total Knee; 4. regard Item Number: 880474001, OR01106A - Knee Arthro
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0550-2023·2023-05-03

    Prescription drug recall for manufacturing quality control deviations

    Northwind Pharmaceuticals is recalling 33 bottles of Doxazosin 4mg tablets due to manufacturing quality control deviations. No illnesses or injuries have been reported.

    Product
    DOXAZOSIN — DOXAZOSIN (DOXAZOSIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1465-2023·2023-05-03

    VersaOne Reusable Positioning Cannula Recalled Due to Internal Metal Burrs

    Covidien LP is recalling VersaOne Reusable Positioning Cannulas (Model RC12STS) due to manufacturing defects that may produce metal burrs on the inside of the device, potentially causing internal tissue damage during use.

    Product
    VersaOne Reusable Positioning Cannula 12mm Standard, Model Number RC12STS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V219000·2023-05-03

    2021 Forest River Berkshire Class A Motorhomes: Brake Light Reflection Defect

    Forest River is recalling certain 2021 Berkshire Class A motorhomes due to brake lights that may not adequately reflect light. The defect affects visibility and compliance with Federal Motor Vehicle Safety Standards.

    Product
    FOREST RIVER — 2021 FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1471-2023·2023-05-03

    Draeger Infinity CentralStation ECG waveform display inaccuracy due to software defect

    Draeger Infinity CentralStation patient monitors may display ECG waveform amplitudes lower than actual values due to a software bug affecting versions VG2.1.3 and lower.

    Product
    Draeger Infinity CentralStation (ICS), centralized monitoring of adult, pediatric and neonatal patient data within the hospital or clinical environment, Software versions VG2.1.3 and lower
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1432-2023·2023-05-03

    Sterile Surgical Kits Recalled Due to Light Handle Cover Separation Risk

    ROi CPS LLC is recalling 662 sterile surgical convenience kits because light handle covers may separate from the light handle and fall off during use. The kits were distributed in Florida and Missouri.

    Product
    Sterile surgical convenience kits: 1. regard Item Number: 880353009, GS00797I - Laparotomy Pk; 2. regard Item Number: 880429002, GS01036B - Universal Custom ; 3. regard Item Number: 800725004, GS00930D - OH Base Robot Pack ; 4. regard Item Number: 800725005, GS00930E - O
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1461-2023·2023-05-03

    GEM NEUROTUBE Nerve Repair Mesh Recalled for Brittleness and Potential Crumbling

    Baxter Healthcare's GEM NEUROTUBE absorbable mesh tube, used for peripheral nerve repair, is recalled because the product is brittle and may crumble when handled or removed from packaging. The recall affects 169 units distributed worldwide.

    Product
    GEM NEUROTUBE, Absorbable Woven Polyglycolic Acid Mesh Tube, Product Codes: a) 5311-01240-010, b) 5311-01240-012; for peripheral nerve repair
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1435-2023·2023-05-03

    Sterile Surgical Kit Light Handle Covers May Separate During Use

    ROi CPS LLC is recalling 386 sterile surgical convenience kits (WPH GYN Laparoscopy Pack) because light handle covers may separate and fall off during use.

    Product
    Sterile surgical convenience kit: regard Item Number: 800753005, GY00958E - WPH GYN Laparoscopy Pack.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0543-2023·2023-05-03

    Peritoneal dialysis solution recalled due to sterility assurance concerns

    Baxter Healthcare Corporation is recalling 9,788 bags of Dianeal Low Calcium with Dextrose peritoneal dialysis solution due to potential leaks in the Luer component. The recall affects Lot Y405201 distributed nationwide in the United States.

    Product
    DIANEAL LOW CALCIUM WITH DEXTROSE — DIANEAL LOW CALCIUM WITH DEXTROSE (SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1470-2023·2023-05-03

    Digital X-ray System Arm May Break, Posing Injury Risk

    FUJIFILM's FDR AQRO digital X-ray system arm may break during use. The tube head support is susceptible to failure, which could cause serious harm to patients or operators.

    Product
    FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system intended for use in general purpose radiography for generating radiographic images of human anatomy, including adult, pediatric, and neonatal exams
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1437-2023·2023-05-03

    Surgical Convenience Kits Recalled Due to Separating Light Handle Covers

    ROi CPS LLC is recalling sterile surgical convenience kits because light handle covers may separate and fall off during use. The affected kits were distributed in Florida and Missouri.

    Product
    Sterile surgical convenience kits: 1. regard Item Number: 800756005, NU00961E - OH Laminectomy Cust Pack; 2. regard Item Number: 880411008, NU01018H - Lumbar Universal ; 3. regard Item Number: 880396007, NU01001G - Craniotomy ; 4. regard Item: 880387005, NU00991E - An
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1464-2023·2023-05-03

    VersaOne Positioning Cannula Recalled for Metal Burr Manufacturing Defect

    Covidien LP recalls VersaOne Reusable Positioning Cannula due to manufacturing defect that may leave a metal burr inside the device. No injuries reported.

    Product
    VersaOne Reusable Positioning Cannula 11mm Standard, Model Number RC11STS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1424-2023·2023-05-03

    Endoscopic Forceps May Fail to Open When Shaft Bent

    Surgical grasping forceps may fail to open when the endoscope shaft is bent, potentially affecting their use during endoscopic procedures.

    Product
    FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 8735.685
    Category
    Medical Device
    Distribution
    Distributed nationwide