The Recall Desk

State

Michigan product recalls

20,322 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.

13926–13950 of 20322

  • SevereCPSC·23735·2023-03-09

    Bedsure Electric Heating Blankets and Pads Recalled for Fire and Burn Hazards

    Bedsure electric heating blankets and pads are recalled because their controllers can malfunction, causing fires and thermal burns. Consumers should stop using them immediately and contact Bedsure for a refund.

    Product
    Bedsure Electric Heating Blankets and Pads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V693000·2023-03-09

    2021 Nissan Versa and Kicks power steering sensor defect

    Nissan is recalling 2021 Versa and Kicks vehicles because an intermittent electrical connection in the power steering torque sensor can disable power steering assist, increasing steering effort and crash risk.

    Product
    NISSAN — 2021 NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23149·2023-03-09

    Kindred Bravely Bamboo Nursing Hoodies Recalled for Choking Hazard

    Akerson Enterprises is recalling about 7,500 Kindred Bravely Bamboo Nursing Hoodies because small plastic caps on the drawcords can be swallowed by nursing babies, creating a choking hazard. No injuries have been reported.

    Product
    Kindred Bravely Bamboo Nursing Hoodies
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23145·2023-03-09

    YETI Soft Coolers and Gear Cases Recalled for Magnet Detachment Risk

    YETI is recalling about 1.9 million soft coolers and gear cases because the magnet-lined closures can fail and detach magnets that pose a risk of serious injury or death if ingested.

    Product
    YETI soft coolers and gear cases
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23148·2023-03-09

    Vornado Air Recalls SRTH Small Room Tower Heaters Due to Fire Hazard

    Vornado Air is recalling about 1,450 SRTH Small Room Tower Heaters due to a manufacturing wiring error that can cause the heater to overheat and pose a fire hazard. No injuries have been reported.

    Product
    SRTH Small Room Tower Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23736·2023-03-09

    Monoprice Pure Outdoor Cooking System Fire Hazard Recall

    Monoprice is recalling about 3,780 Pure Outdoor Cooking Systems because the insulation coating on the stove can ignite during use. Consumers should stop using the product immediately and contact Monoprice for a refund.

    Product
    Pure Outdoor Cooking Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23737·2023-03-09

    Baby Crib Bumpers Recalled for Suffocation Hazard and Federal Ban Violation

    About 125 padded baby crib bumpers sold online from November 2022 through January 2023 are recalled due to suffocation risk. Infants can suffocate if they roll into the bumper and obstruct their breathing; padded crib bumpers are banned under federal law.

    Product
    Baby Crib Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V691000·2023-03-09

    International commercial vehicles recalled for engine connecting rod failure

    Navistar is recalling certain 2018-2021 International HV, HX, LT, and RH vehicles because connecting rod wrist pins may crack, causing engine failure. This could lead to engine shutdown and increase the risk of a crash.

    Product
    INTERNATIONAL — 2018 INTERNATIONAL HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23147·2023-03-09

    Anker 535 Power Banks Recalled Due to Fire Hazard from Battery Overheating

    Fantasia Trading is recalling about 42,000 Anker 535 Power Banks (PowerCore 20k, model A1366) because their lithium-ion batteries can overheat and pose a fire hazard. The firm has received 10 reports of overheating incidents, including one report of minor injuries.

    Product
    Anker 535 Power Banks (PowerCore 20k)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23151·2023-03-09

    Vaunn Medical Adult Bed Rails Recalled for Entrapment and Asphyxia Risk

    BeyondMedShop is recalling approximately 102,000 Vaunn Medical Bed Assist Rail bed rails due to risk of user entrapment and asphyxiation. Users can become trapped within the rail or between the rail and mattress.

    Product
    Vaunn Medical Bed Assist Rail adult bed rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V750000·2023-03-09

    2020-2021 Mazda CX-9 second-row seat may slide forward in crash

    Mazda is recalling certain 2020-2021 CX-9 vehicles with 60/40 split bench second-row seats. The left-side second-row seat may unexpectedly slide forward during a crash, increasing injury risk to occupants.

    Product
    MAZDA — 2020 MAZDA CX-9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1140-2023·2023-03-08

    Life2000 Hospital Ventilator Recalled for Potential Patient Desaturation Risk

    Baxter Healthcare is recalling 135 Life2000 ventilators nationwide due to potential patient desaturation when connected to an oxygen concentrator.

    Product
    Life2000 Ventilator PKG, Hospital, a) REF BT20007, b) REF BT-20-0007, ventilatory support for the care of individuals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1142-2023·2023-03-08

    Life2000 Ventilator poses oxygen desaturation risk with oxygen concentrators

    The FDA recalls Baxter's Life2000 Ventilator due to potential patient desaturation when connected to an oxygen concentrator. Affects 71 units nationwide.

    Product
    Life2000 Ventilator , REF MS-01-0118, ventilatory support for the care of individuals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0453-2023·2023-03-08

    PrimeZEN Black 6000 Capsule Recalled for Undeclared Pharmaceutical Ingredients

    The FDA is recalling PrimeZEN Black 6000 capsules distributed nationwide because they contain undeclared sildenafil and tadalafil. The product is unapproved and was marketed without FDA authorization.

    Product
    PrimeZEN Black 6000 capsule, 2000mg, Male Sexual Performance Enhancement, 1-count blister card, Distributed by: Prime Premier Group, Los Angeles, CA 90006, UPC 7 28175 52189 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1141-2023·2023-03-08

    Life2000 Hospital Ventilator Recalled for Patient Desaturation Risk

    Baxter Healthcare is recalling 8 Life2000 Hospital Ventilator systems due to potential patient desaturation events when the device is connected to an oxygen concentrator.

    Product
    Life2000 Ventilator PKG, Hospital, a) REF BT200011, b) REF BT-20-0011, ventilatory support for the care of individuals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V546000·2023-03-08

    2023 Ford Bronco Transmission Park System Defect Rollaway Risk

    Ford is recalling certain 2023 Bronco vehicles because the transmission park system may be damaged during assembly, preventing the parking pawl from fully engaging. This can result in vehicle rollaway, increasing crash risk.

    Product
    FORD — 2023 FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V549000·2023-03-08

    2024 Chevrolet Silverado and GMC Sierra Steering Gear Fracture Recall

    General Motors is recalling certain 2024 Silverado and Sierra trucks because the steering gear shaft may fracture and disconnect, potentially causing total loss of steering control. Dealers will inspect and replace the steering gear free of charge.

    Product
    CHEVROLET — 2024 CHEVROLET SILVERADO 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1139-2023·2023-03-08

    Life2000 Ventilator System Recall: Risk of Patient Desaturation

    Baxter Healthcare is recalling 4,279 Life2000 Ventilator Systems due to potential patient desaturation when connected to oxygen concentrators.

    Product
    Life2000 Ventilator System, a) REF BT-20-0002, b) REF BT-20-0002A, ventilatory support for the care of individuals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0362-2023·2023-03-08

    Phenylephrine injection recalled due to lack of sterility assurance

    Nephron Sterile Compounding Center is recalling Phenylephrine HCl injection nationwide due to lack of assurance of sterility. Lot PS2008A with expiration 03/07/2023 is affected.

    Product
    Phenylephrine HCl in 0.9% Sodium Chloride Injection, USP, 50 mg/250 mL (200 mcg/mL), 250 mL Single-Dose Container bottle, packaged in 15 x 1 IV Bottles per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC 69374-321-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V548000·2023-03-08

    Travel Trailer Emergency Exit Window May Be Missing

    Highland Ridge is recalling certain 2023-2024 Range Lite Air travel trailers that may lack a secondary emergency exit window. The missing window could prevent occupants from exiting during an emergency.

    Product
    HIGHLAND RIDGE TT — 2024 HIGHLAND RIDGE TT RANGE LITE AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1191-2023·2023-03-08

    Stryker Hoffmann LRF Transport Strut Locking Mechanism Recall

    Stryker is recalling Hoffmann LRF Transport Strut devices due to oversized thread pitch that prevents the distal ring fixation from locking, affecting 488 units nationwide.

    Product
    stryker Hoffmann LRF, Transport Strut, Model Number 4933-0-400; Orthopedic external fixation device intended to keep bone fragments/segments in a correct anatomical position until reliable bone consolidation is achieved
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1170-2023·2023-03-08

    Bone fixation plates recalled due to product packaging mix-up

    Wright Medical Technology is recalling ORTHOLOC 3DSi CLAW II bone fixation plates due to packaging mix-up in specific lots. Packages contained incorrect product codes.

    Product
    ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1173-2023·2023-03-08

    Surgical Sutures Recalled Due to Sterile Barrier Breach Risk in Ophthalmic Procedures

    Covidien LP is recalling 12,732 units of surgical sutures (nylon and silk, McKesson brand) due to a sterile barrier breach in the breather pouch. The breach may cause infection or vision loss when used in eye surgery procedures.

    Product
    Monofilament Nylon Suture (McKesson Branded) and Coated Braided Silk Suture (McKesson Branded) (1) S661GX 5-0 NYLON 18 DS18 (2)S683GX 4-0 SILK 18 DS18 (3) S683GX 4-0 SILK 18 DS18 (4)S697GX 6-0 NYLON 18 DSM11 (5)S697GX 6-0 NYLON 18 DSM11
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1201-2023·2023-03-08

    Medical Device Middleware: MYLA Software Fails to Apply AST Filter Rules

    Biomerieux MYLA laboratory middleware may fail to apply activated antibiotic susceptibility test (AST) filter rules when sending results to clinicians. The defect affects VITEK MS users with versions 4.8.x and 4.9.

    Product
    MYLA comprises AST Filters in conjunction with VITEK MS; middleware which connects microbiology laboratory instruments for ID/AST and blood culture activities and the laboratory information system (LIS).
    Category
    Medical Device
    Distribution
    Distributed nationwide