The Recall Desk

State

Massachusetts product recalls

20,304 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.

11201–11225 of 20304

  • HighFDA (Devices)·Z-0318-2024·2023-11-22

    Express Dry Seal Chest Drains Recalled for Insufficient Setup Instructions

    Atrium Medical Corporation is recalling Express Dry Seal Chest Drains (models 4000-100N and 4050-100N) due to inadequate instructions for proper catheter and patient tube connection setup. No injuries have been reported.

    Product
    Express Dry Seal Chest Drains (Express): 4000-100N DRAIN, EXPRESS, SINGLE; 4050-100N DRAIN, EXPRESS, BRU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0307-2024·2023-11-22

    Medical Device Recall: KWIKSTIK Microbiological Reagent Contaminated with Aspergillus

    Microbiologics Inc recalls KWIKSTIK microbiological reagent kits due to Aspergillus flavus contamination in bulk pellets. Affected products were distributed worldwide, including the US, Italy, France, Turkey, Peru, and Mexico.

    Product
    KWIKSTIK, P. venetum, Catalog numbers: a) 0794P (2-pack), b) 0794K (6-pack)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0294-2024·2023-11-22

    CT Scanner Image Fusion Software Error Affecting Radiation Therapy Planning

    A software bug in Philips Brilliance CT scanners causes image-fusion errors, resulting in incorrect radiation therapy coordinates and potential treatment planning failures.

    Product
    Brilliance CT Big Bore Oncology with software version V4.8.0.10421 Model:728243 CT scanner and simulator designed for radiation oncology and therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0314-2024·2023-11-22

    Blood culture kit recalled due to expired internal components

    Medline's blood culture kit is being recalled because components inside the kit have expired before the kit's stated expiration date. This could affect the kit's ability to function properly.

    Product
    BLOOD CULTURE KIT, REF DYNDH1647B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·24716·2023-11-22

    PandaEar Stainless Steel Toddler Cups Recalled for Excessive Lead Content

    PandaEar Stainless Steel Toddler Cups are being recalled because their exterior solder contains lead levels that exceed federal limits. About 1,600 cups sold on Amazon from May through August 2023 are affected. No injuries have been reported.

    Product
    PandaEar Stainless Steel Toddler Cups, 8 oz.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0298-2024·2023-11-22

    LIFEPAK 15 Defibrillator Recall: Loose Battery Pins May Cause Power Failure

    Physio-Control is recalling LIFEPAK 15 defibrillators due to loose battery pins that may cause power failure. Users should verify device functionality immediately.

    Product
    LIFEPAK 15, REF: 99577-000061, Part Number V15-2-000067
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0316-2024·2023-11-22

    Ocean Chest Drains Recalled for Inadequate Assembly Instructions

    Atrium Medical recalls Ocean chest drains due to insufficient precaution instructions for proper catheter and tube connection setup. Improper assembly could compromise device function.

    Product
    Ocean Water Seal Chest Drains (Ocean): Products REF Number Product Name (1)2002-000 DRAIN, OCEAN SINGLE W/AC,S; (2)2002-040 DRAIN, OCEAN SINGLE,PEDI CONNECTOR; (3)2002-100 DRAIN, OCEAN SINGLE W/AC; (4)2002-300 DRAIN, OCEAN SINGLE W/S; (5) 2002-400 DRAIN, OCEAN SINGLE ;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0302-2024·2023-11-22

    LIFEPAK 15 Defibrillator Recalled for Loose Battery Pins Causing Power Loss

    Physio-Control is recalling LIFEPAK 15 defibrillators due to a potential for battery pins to become loose, which could cause power failure.

    Product
    LIFEPAK 15, REF: 99577-001956, Part Number V15-7-000021
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0300-2024·2023-11-22

    LIFEPAK 15 Defibrillator Recall: Loose Battery Pins Risk Power Loss

    Physio-Control is recalling LIFEPAK 15 defibrillators due to a potential defect where battery pins may become loose, causing power issues.

    Product
    LIFEPAK 15, REF: 99577-001373, Part Number V15-7-000002
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0309-2024·2023-11-22

    Medical Device Reagent Recalled for Unreliable Test Results

    Beckman Coulter's Transferrin reagent lot 2573 does not maintain stability as claimed, causing unreliable patient test results and control failures. The company confirmed the issue affects diagnostic accuracy.

    Product
    AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their size, shape and concentration. Turbidimeters measure the reduction of incident light due to reflection, absorption, or scatter. In the procedure, the measurement
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·24031·2023-11-22

    Lenovo USB-C Laptop Power Banks Recalled for Fire Hazard

    Lenovo is recalling about 2,850 USB-C laptop power banks because internal screws can loosen, causing a short circuit and lithium-ion battery overheating. One fire with minimal property damage has been reported.

    Product
    Lenovo USB-C Laptop Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0223-2024·2023-11-22

    Siemens Mobilett Mira wireless x-ray systems recalled for buzzer mounting defect

    Four Siemens Mobilett Mira wireless mobile x-ray systems are recalled due to incorrect buzzer component mounting that prevents acoustic signals during x-ray activation. The systems remain fully functional with visual LED indicators available for operator monitoring.

    Product
    Mobilett Mira wireless (VA20) mobile x-ray system(s)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateCPSC·24030·2023-11-22

    Balloon Time Mini Helium Tanks Recalled Due to Projectile Injury Risk

    Approximately 121,100 Balloon Time Mini Helium Tanks are being recalled because compressed helium can escape and cause the plastic cap to be ejected, potentially striking users or bystanders. No injuries have been reported.

    Product
    Balloon Time Mini Helium Tanks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24028·2023-11-21

    ZLINE RG Gas Ranges Recalled for Carbon Monoxide Hazard

    ZLINE is recalling about 30,000 RG gas ranges (30-inch, 36-inch, and 48-inch models) because the oven can emit dangerous levels of carbon monoxide, posing a serious risk of injury or death.

    Product
    ZLINE 30-inch, 36-inch and 48-inch RG gas ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24715·2023-11-16

    Target Recalls Hearth & Hand Toy Mushroom Peg Sorters Due to Choking Hazard

    Target is recalling about 1,850 units of its 13-Piece Toy Mushroom Peg Sorters because the mushroom stems can detach, posing a choking hazard to young children. No injuries have been reported.

    Product
    13-Piece Toy Mushroom Peg Sorters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24714·2023-11-16

    LAOION Children's Cups Recalled for Lead Content and Lid Hazards

    LAOION children's cups sold on Amazon contain lead in solder on the cup bottom and have lids that can crack, creating choking and laceration risks. About 200 units were sold from March to May 2023.

    Product
    LAOION Children's Cups
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24026·2023-11-16

    Tractor Supply Red Shed Hammock Swing Chairs Recalled Due to Fall Hazard

    Tractor Supply is recalling about 7,500 Red Shed® Hammock Swing Chairs because the plastic buckle supporting the back can break while someone is seated, causing a fall. The company has received 13 reports of buckle or stitching failures, including three falls.

    Product
    Red Shed® Hammock Swing Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24027·2023-11-16

    Khaite Women's High Heeled Sandals Recalled for Detaching Heels and Fall Risk

    Khaite is recalling approximately 1,860 women's high heeled sandals from its Spring Summer 2024 collection because the heels can detach, creating a fall hazard. Consumers should stop using the shoes immediately and contact Khaite for a refund.

    Product
    Women's high heeled sandals (Spring Summer 2024 collection, Louisa, Linden and Seigel Heel Sandals)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0102-2024·2023-11-15

    Pfizer Lidocaine Injection Recall: Glass Particulates in Injectable Medication

    Pfizer is recalling 3,200 vials of Lidocaine Hydrochloride 2% Injection due to the presence of glass particulates. The injectable medication was distributed nationwide in the US and Puerto Rico.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0194-2024·2023-11-15

    FDA Recalls Olympus EVIS EXERA III Bronchovideoscope for Combustion Risk

    Olympus Corporation is recalling 3,948 EVIS EXERA III bronchovideoscope units nationwide due to risk of combustion during electrosurgical procedures when high-frequency cauterization is used with oxygen supply.

    Product
    EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS Model Number BF-P190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0101-2024·2023-11-15

    Lidocaine injection recalled due to glass particulate matter

    Pfizer Inc. is recalling 21,390 vials of Lidocaine Hydrochloride 1% injection due to presence of glass particulate matter. Lot 42290DK with expiration 6/1/2024 is affected.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0189-2024·2023-11-15

    Five Olympus Bronchovideoscope Models Recalled for Endobronchial Combustion Risk

    Olympus is recalling 15,942 bronchovideoscope units nationwide due to endobronchial combustion risk during cauterization procedures with oxygen supply. The hazard occurs when the electrode of the surgical accessory is positioned too close to the scope's distal end.

    Product
    BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Numbers BF-1T150, BF-1T60, BF-P150 BF-P60 and EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Number XT160
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0188-2024·2023-11-15

    StealthStation S8 Surgical Navigation System Software Anomaly Recall

    Medtronic is recalling StealthStation S8 and FlexENT systems with software versions 2.0 and 2.0.1 due to a software anomaly that could cause surgical planning data to shift to an unintended location.

    Product
    StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The StealthStation System, with StealthStation Cranial software, is intended as an aid for locating anatomical structures in either open or percutaneous neurosurgical procedures. The StealthStation FlexENT
    Category
    Medical Device
    Distribution
    Distributed nationwide