State
20,199 recalls have nationwide distribution and so reach Michigan. 0 additional recalls listed Michigan specifically in their distribution scope.
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.
Stryker Medical is recalling ProCuity bed series model 3009 due to missing electrical safety test values. The beds pose a risk of electrical shock or tissue burn to patients.
Thor Photomedicine is recalling 19 NovoTHOR Gen 2.0 red light therapy beds due to ball stud component failures that can cause canopy detachment or difficulty in lifting. The beds were distributed worldwide.
Thor Photomedicine is recalling six THOR NOVO GEN 2.0 XL whole body red light therapy beds due to ball stud component failure. The defect causes gas strut detachment, making the canopy difficult to lift.
Encore Medical is recalling 37 DJO surgical EMPOWR Porous Knee System SIZE 8 devices distributed nationwide because incorrect product components were packaged with certain units.
Stryker is recalling ProCuity patient beds (model 3009) for missing required electrical safety test documentation, creating a risk of electrical shock or tissue burn.
Randox is recalling RANDOX Total Bilirubin reagent because reports indicate elevated patient results when using plasma samples with this reagent.
STAQ Pharma is recalling ROPivacaine HCl 0.2% injection bags nationwide due to leaking bags caused by manufacturing quality control failures. No illnesses or injuries have been reported.
Ortho-Clinical Diagnostics is recalling certain VITROS ECO2 diagnostic slides that may produce inaccurate carbon dioxide measurements, potentially leading to misdiagnosis of acid-base balance disorders.
BioFire Diagnostics is recalling BIOFIRE Blood Culture Identification 2 (BCID2) Panels due to instrument characteristic changes that cause Candida tropicalis to be detected but reported as 'Not Detected' in quality control testing.
Liberty Medical Solutions is recalling 473 Multi-Mode TENS stimulator units distributed in five states due to missing warnings and contraindications in instruction manuals.
Sun Pharmaceutical is recalling Bupropion Hydrochloride Extended-Release Tablets 200 mg due to failed dissolution specifications. The recall affects 2,016 bottles with lot HAD0630A distributed nationwide.
Right Value Drug Stores is recalling LET Gel topical anesthetic syringes nationwide due to incorrect product formulation. Patients should not use affected syringes and should consult their healthcare provider.
Luminex Corporation is recalling 222 kits (4,440 VERIGENE BC-GP Utility Trays) used in blood culture testing due to potentially defective utility trays. The affected lot (062123018C) expires December 20, 2023.
Tesla is recalling 2.03 million 2012-2023 Model S/X/3/Y vehicles with Autosteer due to insufficient control prominence that may allow driver misuse and crash risk. A free OTA software update will be provided.
General Motors is recalling certain 2023 Cadillac Lyriq vehicles due to a software defect in the body control module. The pedestrian warning sounds may fail to activate, creating a crash risk.
Southeast Toyota Distributors is recalling certain 2023 Toyota 4Runner vehicles due to an incorrect load carrying capacity modification label. The error could result in vehicle overloading and increased crash risk.
General Motors is recalling 2023 GMC Acadia vehicles and certain 2024 Cadillac models due to windshields that may not be properly bonded to the vehicle body. A detached windshield during a crash could increase the risk of injury.
XpressGoods is recalling colorful neodymium magnetic balls that exceed federal safety limits for toy magnets. When swallowed, the magnets can lodge in the digestive system and cause serious injury or death.
Segway Powersports is recalling about 1,100 2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles because the ignition coil can fail, allowing fuel to enter the exhaust pipe and ignite, creating a fire hazard. One vehicle fire with property damage has been reported.
Toyota and Lexus are recalling approximately 152,927 vehicles with defective steering column welds that can deactivate the driver's air bag, increasing crash injury risk.
Moonsea Pack and Play Mattresses sold on Amazon violate federal crib mattress safety regulations and pose a suffocation hazard to infants. Consumers should stop using them immediately and contact Moonseasleep for a refund.
SourceOne Ventures recalls Windsor Queen Xtrabed Mobile Murphy Beds due to risks of cabinet breakage and tip-over. About 12,000 units sold at Wayfair between November 2016 and April 2023 are affected.
Jayco is recalling certain 2021-2022 Seneca recreational vehicles because the windshield wiper arms may fail, reducing driver visibility and increasing crash risk. Owners should contact Jayco customer service at 1-800-283-8267 for a free inspection and replacement.
Adven Group LLC is recalling about 1,540 Nap Queen 12-inch Maxima Hybrid Mattresses sold via Amazon, Walmart, and Overstock because they fail to meet federal flammability standards and pose a fire hazard.
Wet & Forget USA is recalling about 2.7 million bottles of "Xtreme Reach" Outdoor Mold & Mildew Stain Remover with hose end nozzles. The nozzle clip can dislodge, spraying cleaning solution on users and causing skin and eye irritation.