The Recall Desk

State

Massachusetts product recalls

20,188 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.

8651–8675 of 20188

  • HighCPSC·24291·2024-07-03

    Hatch Baby Power Adapters for Rest 1st Generation Sound Machines Pose Shock Hazard

    Hatch Baby is recalling power adapters sold with Rest 1st Generation sound machines because the plastic housing can detach from the adapter when unplugged, exposing electrical prongs and creating a shock hazard. The firm has received 19 reports of the housing coming off, including two reports of minor electrical shock.

    Product
    Power Adapters sold with Rest 1st Generation sound machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2167-2024·2024-07-03

    FDA Recalls CUSA Excel Surgical Handpiece for Housing Cracks

    Integra LifeSciences is recalling CUSA Excel C2600 surgical handpieces due to potential housing cracks that may delay treatment. The recall affects 2,652 units distributed nationwide and internationally.

    Product
    CUSA Excel C2600 23KHz Straight Handpiece-Indicated for use in surgical procedures where fragmentation, emulsification and aspiration of soft and hard tissue Catalog Number: C2600* *Note: you may see C2600P or C2600SRL on labeling. This notice is applicable for those SKUs as w
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1427-2024·2024-07-03

    Cream Cheese Stuffed Plain Mini Bagels Recalled for Undeclared Gluten

    FEEL GOOD FOODS INC is recalling Cream Cheese Stuffed Plain Mini Bagels due to undeclared gluten. Consumers with gluten sensitivity or celiac disease should not consume this product.

    Product
    Cream Cheese Stuffed Plain Mini Bagels
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2209-2024·2024-07-03

    Implantable defibrillator recalled for manufacturing defect causing device failure risk

    Medtronic is recalling five implantable defibrillators due to a manufacturing defect where weld cracks caused devices to fail quality testing. The defective devices were identified during manufacturing and did not reach patients.

    Product
    Cobalt XT DR MRI SureScan, Model Number DDPA2D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2206-2024·2024-07-03

    Medtronic COBALT DR MRI ICD Recalled for Manufacturing Defect

    Nine Medtronic COBALT DR MRI implantable cardioverter defibrillators are recalled due to a weld crack that caused devices to fail manufacturing quality checks.

    Product
    COBALT DR MRI SureScan, Model Number DDPB3D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2181-2024·2024-07-03

    Siemens X-ray Table Recalled for Fire Hazard in Power Supply

    Siemens recalls AXIOM MULTIX MT radiographic X-ray tables due to a short circuit in the power supply unit that may cause overheating and fire. 7 units are affected nationwide.

    Product
    AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395415
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2220-2024·2024-07-03

    CDC Influenza H5 Subtyping Kit may produce inconclusive test results

    The CDC Influenza A/H5 Subtyping Kit's H5b component may fail to amplify, resulting in inconclusive results. 191 units were distributed nationwide.

    Product
    CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2178-2024·2024-07-03

    Sonic Scaler Tip Holder May Be Oversized, Preventing Proper Seating

    The tip holder portion of Titan Blis-Sonic Scaler tips may be oversized, preventing proper seating in the scaler handpiece. This defect could result in the tip becoming loose during use.

    Product
    Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Perio (part number 261669) (1) P/N 264563 (2) P/N 264565 The scaler tip is used with an air drive scaler for subgingival scaling and fine access. The Perio tip is used for lingual supragingival scaling of mandibu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0569-2024·2024-07-03

    SinuFrin Nasal Decongestant Recalled for Sub-Potency Nationwide

    NeilMed Pharmaceuticals is recalling 20,370 bottles of SinuFrin Quick Relief Decongestant (Lot SD134) nationwide due to sub-potency. No illnesses have been reported.

    Product
    SINUFRIN QUICK RELIEF DECONGESTANT — SINUFRIN QUICK RELIEF DECONGESTANT (SINUFRIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V077000·2024-07-02

    2024 Kia Telluride recalled for engine valve spring failure

    Kia is recalling certain 2024 Telluride vehicles because engine valve springs may break while driving. This could cause loss of drive power and increased risk of fire.

    Product
    KIA — 2024 KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V013000·2024-07-01

    2022 Chevrolet Equinox fuel pump module may cause engine stall

    General Motors is recalling certain 2021-2022 Chevrolet Equinox and 2022 GMC Terrain vehicles because the fuel pump module may not provide sufficient fuel to the engine, causing it to stall and increasing crash risk.

    Product
    CHEVROLET — 2022 CHEVROLET EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24744·2024-06-27

    Dania Furniture Recalls Hayden Bookcase Due to Tip-Over Hazard

    Dania Furniture is recalling about 940 Hayden Bookcases sold from November 2017 through February 2024 because the bookcase can tip over and cause entrapment injuries if not anchored to the wall. A 4-year-old child died from a tip-over incident in August 2023.

    Product
    Hayden Bookcase
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24287·2024-06-27

    Baseus Magnetic Wireless Charging Power Banks Recalled for Fire Hazard

    Shenzhen Baseus Technology is recalling about 132,000 Baseus Magnetic Wireless Charging Power Banks because the lithium-ion batteries can overheat, posing a fire hazard. The company has received 171 incident reports including 39 fires, 13 burn injuries, and about $20,000 in property damage.

    Product
    Baseus Magnetic Wireless Charging Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24285·2024-06-27

    Brookstone TurboVac Handheld Rechargeable Vacuums Recalled for Fire Hazard

    Southern Telecom is recalling about 10,600 Brookstone TurboVac handheld rechargeable vacuums (Model BSBVAC301) due to a fire hazard caused by battery short circuits during or after charging. The firm has received two reports of serious fires resulting in property damage.

    Product
    Brookstone TurboVac Handheld Rechargeable Vacuums
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24284·2024-06-27

    At Home Recalls Tie Dye Fur Toy Trunk Storage Chests for Entrapment Risk

    At Home Procurement is recalling approximately 990 Tie Dye Fur Toy Trunk Storage Chests sold from September 2023 through February 2024 because they lack a lid support feature and ventilation holes, creating entrapment and suffocation hazards.

    Product
    Tie Dye Fur Toy Trunk Storage Chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24283·2024-06-27

    REI Co-op Cycles REV Children's Bicycles with Training Wheels Recall

    REI is recalling Co-op Cycles REV children's bicycles (12-, 16-, and 20-inch models, 2022-2024) because the training wheel assembly knob can loosen and detach, creating fall and injury hazards.

    Product
    Co-op Cycles REV 12-, 16-, or 20-inch Kid's Bicycles with training wheels (all model years 2022-2024)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24286·2024-06-27

    Daikin, Amana, and Goodman Heat Pumps Recalled for Excessive Heat Risk

    Daikin Comfort Technologies is recalling about 56,000 Daikin FIT, Amana Brand S-series, and Goodman SD heat pumps due to a power interruption defect that can cause the units to provide heat even when the thermostat is set to cooling mode, posing a risk of excessive heat exposure.

    Product
    Daikin FIT, Amana Brand S-series, and Goodman SD heat pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2020-2024·2024-06-26

    Ventilator HAMILTON-C6 may fail to restart, risking oxygen deprivation

    Hamilton Medical AG is recalling the HAMILTON-C6 ventilator due to a sensor failure that may prevent re-initiation after reconnection, potentially causing hypoxia.

    Product
    Ventilator HAMILTON-C6, PN: 160021
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2130-2024·2024-06-26

    Ventilator Operator's Guide Recalled for Missing Critical MRI Safety Information

    ZOLL is recalling operator's guides for the ZOLL 731 Ventilator because they omit critical MRI safety information. Missing distance guidance could cause the ventilator to malfunction during MRI procedures.

    Product
    ZOLL 731 Ventilator (EMV+, AEV, Eagle II) - for MRI Compatible Devices - Operator's Guide and Quick Reference Guide (QRGs) as follows: Part Numbers: 1. 799-EGL2-02 2. 799-EGL2-02-01 3. 799-EGL2-02-04 4. 799-EGL2-02-05 5. 799-EGL2-02-08 6. 799-EGL2-02-10 7. 799-EGL2-02-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2144-2024·2024-06-26

    VICRYL Sutures recalled due to packaging defect compromising sterility

    Ethicon recalls 341,532 units of VICRYL surgical sutures worldwide due to holes in primary packaging that compromise sterility and could result in infection.

    Product
    VICRYL (polyglactin 910) Suture - Indicated for use in general soft tissue approximation and/or ligation, including use in ophthalmic surgery, but not for use in cardiovascular and neurological tissues. PRODUCT CODE: J214H J218H J258H J268H J269H J327H J344H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2147-2024·2024-06-26

    PDS Plus Antibacterial Surgical Sutures Recalled for Compromised Sterility

    Ethicon recalls PDS Plus Antibacterial sutures due to packaging defects that compromised sterility. The affected units may cause infection if used in surgery.

    Product
    PDS Plus Antibacterial (polydioxanone) Suture - Intended for use in general soft tissue approximation, including use in paediatric cardiovascular tissue, in microsurgery and in ophthalmic surgery. These sutures are particularly useful where the combination of an absorbable suture
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2145-2024·2024-06-26

    FDA Recalls VICRYL Plus Antibacterial Sutures Due to Packaging Defect

    Ethicon is recalling VICRYL Plus Antibacterial Sutures due to a packaging machine defect that created holes in the primary packaging, potentially compromising product sterility. Affected sutures may pose an infection risk.

    Product
    VICRYL Plus Antibacterial (polyglactin 910) Suture - Indicated for use in general soft tissue approximation and/or ligation, except for ophthalmic, cardiovascular and neurological tissues. PRODUCT CODE: VCP196H VCP417H VCP602H VCP603H VCP662H VCPB259H VCPB94
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0559-2024·2024-06-26

    Cefixime Oral Suspension Recalled for Failed Content Uniformity Specifications

    Lupin Pharmaceuticals is recalling one lot of Cefixime oral suspension (200 mg/5 mL) due to failed content uniformity specifications. The recall affects 3,552 bottles distributed nationwide.

    Product
    CEFIXIME — CEFIXIME (CEFIXIME)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2146-2024·2024-06-26

    PDS II Polydioxanone Sutures Recalled Due to Compromised Sterility

    Ethicon is recalling 56,952 units of PDS II polydioxanone sutures distributed worldwide because a packaging defect resulted in compromised sterility, which could lead to infection. No illnesses have been reported.

    Product
    PDS II (polydioxanone) Suture - Intended for use in general soft tissue approximation, including use in paediatric cardiovascular tissue, in microsurgery and in ophthalmic surgery. These sutures are particularly useful where the combination of an absorbable suture and extended wo
    Category
    Medical Device
    Distribution
    Distributed nationwide