The Recall Desk

State

Massachusetts product recalls

20,324 recalls have nationwide distribution and so reach Massachusetts. 0 additional recalls listed Massachusetts specifically in their distribution scope.

About recalls in Massachusetts

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 Massachusetts 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 20324

  • HighNHTSA·21V840000·2023-03-10

    Hyundai recalls 2021 Palisade for brake fluid contamination

    Brake fluid contamination in certain 2021 Hyundai Palisades can reduce braking performance and increase crash risk. Owners should contact Hyundai for a free brake system repair.

    Product
    HYUNDAI — 2021 HYUNDAI PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23150·2023-03-09

    Calico Critters Animal Figures Recalled Due to Choking Hazard; Two Deaths Reported

    Epoch Everlasting Play is recalling more than 3.2 million Calico Critters animal figures and sets sold with bottle and pacifier accessories due to choking hazard. Two fatal incidents have been reported.

    Product
    Calico Critters® Animal Figures and Sets sold with Bottle and Pacifier Accessories
    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
  • 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
  • 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
  • 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
  • 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·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·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·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
  • 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
  • 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·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
  • 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
  • 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
  • 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-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
  • 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
  • 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-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
  • 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-1195-2023·2023-03-08

    Vascular Diagnostic Device Recalled for Risk of Air Line Misconnection

    Unetixs Vascular recalls MultiLab Series II ROODRA vascular diagnostic devices due to luer fittings that may allow air line misconnection to intravenous lines, potentially causing air embolism.

    Product
    MultiLab Series II ROODRA non-invasive vascular diagnostic device, Model Number 11986-0000-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0361-2023·2023-03-08

    Phenylephrine HCl Injection Recalled for Sterility Assurance Deficiency

    Nephron is recalling 24,870 Phenylephrine HCl Injection vials nationwide due to lack of sterility assurance. No illnesses have been reported.

    Product
    Phenylephrine HCl Injection, USP, 0.8 mg/10 mL (80 mcg/mL), 10 mL Single-Dose Vial, packaged in 30 x 10 mL Single-Dose Vials per carton, 12 x 30 Vials Carton per case, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC 69374-301-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1185-2023·2023-03-08

    Medivac Guardian blood loss estimation device inserts may provide inaccurate readings

    Stryker's Medivac Guardian 3L scanning labels may cause inaccurate blood loss estimates, potentially delaying treatment for postpartum hemorrhage. The recall affects 541 units distributed nationwide.

    Product
    Finished Goods Box of 50 Inserts and Scanning Labels for Medivac Guardian 3L Catalog Number: FG 12022. Intended adjunct in the estimation of blood loss.
    Category
    Medical Device
    Distribution
    Distributed nationwide