The Recall Desk

State

Michigan product recalls

20,324 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.

14226–14250 of 20324

  • HighFDA (Devices)·Z-1067-2023·2023-02-15

    Sterile Procedural Trays Recalled Due to Blade Puncture Risk

    Medline Industries is recalling sterile procedural trays because sterile blades within the kits may puncture the protective foil packaging. Approximately 12,964 cases (23,379 units) distributed worldwide are affected.

    Product
    Sterile Procedural Trays, labeled as the following: a. EP LAB PACEMAKER PACK b. OPEN HEART CDS c. OPEN HEART CDS d. AAA CDS e. OPEN HEART CDS f. PACEMAKER CDS g. HEART CDS h. VALVE PACK i. OPEN HEART CDS-3 j. OPEN HEART PACK k. OPEN HEART PACK l. OPEN HEART ADULT m. OPEN HEART C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1098-2023·2023-02-15

    Zimmer Identity Shoulder Resection Planer Units Recalled for Malfunction

    Zimmer, Inc. is recalling 84 units of the Identity Shoulder System Resection Planer due to defects discovered during training testing. Some units are unusable, potentially affecting surgical performance in shoulder procedures.

    Product
    Identity Shoulder System Resection Planer 35mm Resection Planer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0340-2023·2023-02-15

    Fiber Powder Dietary Supplement Recalled for Cronobacter sakazakii Contamination

    Ortho Molecular Products is recalling fiber powder dietary supplements due to Cronobacter sakazakii detected in raw material. About 4,929 bottles distributed nationwide and to Canada are affected.

    Product
    Fiber Powder, Dietary Supplement, Apple Cinnamon Flavored, packaged under the following brands and sizes. 1. Ortho Molecular Products Fiber Plus, Product #608445, Net Wt. 15.9 oz (450 Grams) UPC 6 15033-00608 2. Ortho Molecular Products, Inc., 3017 Business Park Drive, Stevens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0264-2023·2023-02-15

    Ohm Sanitizer Spray Recalled Due to Chemical Contamination

    Urban Electric Power is recalling Ohm Sanitizer Spray nationwide because FDA analysis found the product contains acetaldehyde and acetal above specification limits.

    Product
    Ohm Sanitizer Spray (alcohol (ethyl alcohol) 80% v/v, 8 FL OZ (237 ML) bottles.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1084-2023·2023-02-15

    Sterile Procedural Trays Recalled Due to Potential Packaging Puncture

    Medline Industries is recalling sterile procedural trays because sterile blades may puncture the outer packaging foil, potentially compromising sterility. No injuries have been reported.

    Product
    Sterile Procedural Trays, labeled as the following: MINOR BASIC PACK-LF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1085-2023·2023-02-15

    Sterile Procedural Trays Recalled Due to Blade Puncture Risk

    Medline Industries is recalling Sterile Procedural Trays (LS MS PACK) because the sterile blade inside can potentially puncture the outer packaging layer, compromising sterility.

    Product
    Sterile Procedural Trays, labeled as the following: LS MS PACK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1077-2023·2023-02-15

    Sterile Surgical Trays Recalled for Blade Puncture of Packaging

    Medline Industries is recalling sterile surgical trays used in plastic and reconstructive surgery because blades within the kits can puncture the outer foil packaging, potentially compromising sterility. Approximately 15,009 units were distributed nationwide and internationally.

    Product
    Sterile Procedural Trays, labeled as the following: a. BREAST AUGMENTATION b. BREAST REDUCTION CDS c. CUH ABDOMINOPLASTY CDS d. ACH PLASTICS BREAST-LF e. NE BREAST RECON CDS f. PLASTIC SURGERY CDS g. MINOR PLASTIC CDS h. GROTH BREAST CDS i. BREAST ABD j. MINOR/U-BAR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1061-2023·2023-02-15

    Sterile Trach Pack procedure kits recalled due to blade puncture risk

    Medline Industries is recalling TRACH PACK sterile procedure kits because sterile blades within the kits can puncture the outer foil packaging, potentially compromising product sterility.

    Product
    TRACH PACK. Sterile Procedural Tray.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1062-2023·2023-02-15

    Medline sterile procedural trays recalled for blade packaging puncture

    Medline is recalling sterile procedural trays (Lot 22IBG550) because sterile blades can puncture the foil packaging, compromising sterility. Units were distributed worldwide.

    Product
    LOCAL PACK. Sterile Procedural Tray.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0265-2023·2023-02-15

    Akorn Atropine Sulfate Eye Solution Recalled for Failed Stability Testing

    Akorn is recalling 45,117 bottles of Atropine Sulfate Ophthalmic Solution because stability testing found viscosity measurements out of specification. The affected product should not be used.

    Product
    Atropine Sulfate Ophthalmic Solution, USP 1%, For Topical Application To The Eye, 2 mL bottle, Sterile, Rx only, Distributed by: Akorn Operating Company LLC, Gurnee, IL 60031. NDC: 17478-215-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1052-2023·2023-02-15

    NuVasive Pulse III Multimodality System remote monitoring connection failure

    An incorrect security key prevents the NuVasive Pulse III system from connecting to remote monitoring during spinal, thoracic, and extremity surgeries. Affected facilities should contact NuVasive for corrective action.

    Product
    NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V928000·2023-02-12

    2022 Ford Bronco Airbag Sensors May Not Secure Properly

    Ford is recalling certain 2022 and 2021 Bronco vehicles because the side impact sensors may not be properly secured. This could cause airbags to deploy unintentionally or fail to deploy in a crash, increasing injury risk.

    Product
    FORD — 2022 FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V923000·2023-02-12

    2022-2023 Chevrolet Malibu Recalled for Defective Front Impact Bar Weld

    General Motors is recalling certain 2022-2023 Chevrolet Malibu vehicles with improperly welded front impact bars. The structural defect may prevent crash sensors from working correctly, increasing the risk of injury in a crash.

    Product
    CHEVROLET — 2022 CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V735000·2023-02-11

    2023-2024 Honda Pilot steering rack defect may cause loss of steering control

    Honda is recalling certain 2023-2024 Pilot vehicles due to a loose ball bearing in the steering rack gearbox assembly. This defect can result in loss of steering control or steering lock-up, increasing crash risk.

    Product
    HONDA — 2023 HONDA PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V665000·2023-02-10

    2024 Holiday Rambler Invicta Motorhome Griddle Fire Hazard Recall

    REV Recreation Group is recalling certain 2024 Holiday Rambler Invicta motorhomes. The exterior griddle may be stowed while still connected to the LP gas line, creating a fire risk.

    Product
    HOLIDAY RAMBLER — 2024 HOLIDAY RAMBLER INVICTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23726·2023-02-09

    E-Z-GO Personal Transportation Vehicles Recalled for Fire Hazard

    Textron Specialized Vehicles is recalling about 143,000 E-Z-GO personal transportation vehicles because the electronic board powering the USB port can overheat and ignite, creating a fire hazard. Consumers should stop using the vehicles immediately and contact Textron for a free repair.

    Product
    E-Z-GO Personal Transportation Vehicles (PTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23116·2023-02-09

    Ovation Protégé Equestrian Helmets Recalled for Impact Injury Hazard

    English Riding Supply is recalling about 49,300 Ovation Protégé equestrian helmets because they fail to meet safety impact standards. Riders who fall face an injury risk.

    Product
    Equestrian helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23725·2023-02-09

    LiftMaster myQ Garage Door Control Panels Recalled for Entrapment Hazard

    Chamberlain Group is recalling about 96,400 LiftMaster myQ garage door control panels because the secondary entrapment protection system can fail, allowing the garage door to close even when an obstruction is present. No injuries have been reported in the U.S.

    Product
    LiftMaster myQ Garage Door Control Panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V686000·2023-02-09

    2022 Ford F-150 Parking Light Flickering Defect Recall

    Ford is recalling 2022 F-150 trucks and 2022-2023 Bronco Sport vehicles due to a lighting control module defect causing parking light flickering when headlights are activated. The flickering reduces visibility and increases crash risk.

    Product
    FORD — 2022 FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23118·2023-02-09

    IKEA ODGER Swivel Chairs Recalled Due to Leg Base Breakage and Fall Risk

    IKEA is recalling about 12,000 ODGER Swivel Chairs in anthracite because the leg base can break, creating a fall hazard. Four reports of leg base breaking have been received, including two reports of consumer injuries from falls.

    Product
    IKEA ODGER Swivel Chairs, Anthracite
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V687000·2023-02-09

    2022 Volkswagen Taos Engine Stall Software Safety Recall

    Volkswagen is recalling certain 2022 Taos vehicles with all-wheel drive due to engine control unit software that may cause engine stall when coming to a stop, increasing crash risk. Dealers will provide free software updates.

    Product
    VOLKSWAGEN — 2022 VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23117·2023-02-09

    Skip Hop Silver Lining Cloud Activity Gyms Recalled for Choking Hazard

    Skip Hop is recalling Silver Lining Cloud Activity Gyms because raindrops attached to the included cloud toy can detach and pose a choking hazard to children. No injuries have been reported.

    Product
    Silver Lining Cloud Activity Gyms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23723·2023-02-09

    Model Year 2023 Can-Am Side-by-Side Vehicles Recalled for Fire Hazard

    BRP is recalling about 3,310 Model Year 2023 Can-Am side-by-side vehicles because a defective fuel hose assembly could leak fuel and create a fire hazard. Consumers should stop using the vehicles and contact a Can-Am dealer for a free repair.

    Product
    Model Year 2023 Can-Am side-by-side vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide