The Recall Desk

Hazard

Laceration recalls

158 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all laceration recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

26–50 of 158

  • SevereCPSC·25455·2025-09-04

    Makita Cordless Grease Guns Recalled for Laceration Hazard from Hose Rupture

    Makita cordless grease guns and hoses are recalled because the hose can develop holes, allowing pressurized grease to eject and cause lacerations. The company received five reports of laceration injuries worldwide.

    Product
    Makita Professional Cordless Grease Guns and Makita Grease Gun Hoses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25435·2025-08-14

    Drinkmate 1-Liter Carbonation Bottles Recalled Due to Explosion Hazard

    About 106,200 Drinkmate 1L Carbonation Bottles can explode during use, causing lacerations and impact injuries. The company has received eight reports of explosions, including four with reported injuries, and is offering free replacements.

    Product
    Drinkmate 1L Carbonation Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25420·2025-07-31

    IKEA Garlic Presses Recalled for Laceration and Ingestion Hazards

    IKEA is recalling about 43,830 IKEA 365+ VÄRDEFULL garlic presses sold from March to May 2025 because small metal pieces can detach, posing laceration or ingestion hazards. No injuries have been reported in the U.S.

    Product
    IKEA 365+ VÄRDEFULL garlic presses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25414·2025-07-31

    Leatherman Charge Plus Multi-Tools Recalled Due to Laceration Hazard

    About 17,000 Leatherman Charge Plus and Charge Plus TTi multi-tools have a blade tip that doesn't fully fold into the handle, posing a laceration risk. The manufacturer is offering free repairs for affected units.

    Product
    Leatherman Charge Plus and Charge Plus TTi Multi-Tools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25416·2025-07-31

    RIDGID 18V Brushless Framing Nailers Recalled Due to Laceration Hazard

    TTI Consumer Power Tools is recalling about 64,000 RIDGID 18V Brushless Framing Nailers due to a malfunction in the dual action engagement system that can cause involuntary nail discharge, posing a laceration hazard.

    Product
    RIDGID 18Volt Brushless 21-Degree Framing Nailers and RIDGID 18Volt Brushless 30-Degree Framing Nailers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25371·2025-07-03

    Positec Chainsaws and Pole Saws Recalled Due to Failing Switch

    Positec recalls approximately 49,000 Hyper Tough, Worx, and Portland chainsaws and pole saws. A defective power switch can fail to stop the saw, creating a laceration hazard. No injuries reported.

    Product
    Hyper Tough, Worx and Portland Chainsaws and Pole Saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25367·2025-07-03

    DEWALT Grinder Flap Discs Recalled Due to Detachment and Laceration Risk

    DEWALT is recalling about 17,680 grinder flap discs because the ceramic abrasive flaps can detach during use, causing cuts and scrapes. Consumers should stop using the product and follow the manufacturer's recall process for a refund.

    Product
    DEWALT® Grinder Flap Discs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25353·2025-06-26

    Coleman Converta camping cots and stretchers recalled for pinching hazard

    The Coleman Company recalls Converta camping cots and suspension stretchers whose backrest fold mechanism can pinch consumers' fingers. The firm has received 7 reports of pinching injuries, including 2 fractured fingers.

    Product
    Converta camping cots and Converta camping suspension stretchers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25334·2025-06-12

    Cordless Hedge Trimmers Recalled for Unexpected Blade Activation Laceration Risk

    RYOBI 40V Cordless Hedge Trimmers are being recalled because the blade can activate unexpectedly when only one control is pressed instead of both. The defect has caused 16 reported injuries involving lacerations.

    Product
    RYOBI 40V 24-Inch Cordless Hedge Trimmers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1776-2025·2025-05-21

    Philips Intera 1.5T MRI quadrature body coil seal adhesive failure recall

    Philips recalls certain Intera 1.5T MRI machines due to potential failure of the quadrature body coil seal, which may create sharp edges causing patient injury during scans.

    Product
    Intera 1.5T Master/Nova, Model Number: 781106;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1773-2025·2025-05-21

    Philips Intera 1.0T MRI scanner coil seal adhesive failure risk

    Philips recalls the Intera 1.0T Power/Pulsar MRI scanner. The Quadrature Body Coil seal adhesive may fail during scanning, creating sharp edges that could cause skin abrasions, lacerations, hair entanglement, or tissue injury.

    Product
    Intera 1.0T Power/Pulsar, Model Number: 781103;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1772-2025·2025-05-21

    Philips Intera 1.0T MRI Quadrature Coil Seal Adhesive Failure

    Philips is recalling certain Intera 1.0T MRI machines due to a Quadrature Body Coil seal adhesive that may fail and create sharp edges. These edges could contact patients during scanning and cause skin abrasions, lacerations, or tissue injury.

    Product
    Intera 1.0T Omni/Stellar, Model Number: 781102;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1770-2025·2025-05-21

    Philips Enterprise 1.5T MRI Systems Recalled for Potentially Sharp Coil Seal

    Philips recalls certain Enterprise 1.5T MRI systems (Model 781145) due to potential adhesive failure in the Quadrature Body Coil seal that may create sharp edges. These edges could contact patients during scanning and cause skin injuries.

    Product
    Enterprise 1.5T, Model Number: 781145;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1779-2025·2025-05-21

    Philips Intera MRI Scanner Coil Seal May Create Sharp Edges

    Philips Intera 1.5T MRI scanners may develop sharp edges from a failing quadrature coil seal adhesive, risking patient skin injuries during scanning procedures. The recall affects 23 units distributed in the US and internationally.

    Product
    Intera 1.5T R11, Model Number: 781170;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1775-2025·2025-05-21

    MRI Scanner Body Coil Seal Adhesive Failure Creates Risk of Sharp Edges

    Philips Intera 1.5T MRI scanners may have defective quadrature body coil seals. The adhesive can fail and create sharp edges that could injure patients during scanning.

    Product
    Intera 1.5T Explorer/Nova Dual, Model Number: 781108;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1771-2025·2025-05-21

    Philips Intera 0.5T MRI Scanner Recall Due to Sharp Coil Seal Edges

    Philips has recalled 14 Intera 0.5T MRI scanners due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges that could injure patients during scanning.

    Product
    Intera 0.5T Standard, Model Number: 781101;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1780-2025·2025-05-21

    Philips Intera MRI Scanner Coil Seal Adhesive Failure Risk

    The Philips Intera 3.0T Quasar Dual MRI scanner may have a failing quadrature body coil seal adhesive that creates sharp edges, posing risk of skin injuries including lacerations and tissue damage to patients.

    Product
    Intera 3.0T Quasar Dual, Model Number: 781150;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1777-2025·2025-05-21

    Philips Intera 1.5T MRI machines: Quadrature coil seal failure risk

    Philips is recalling 26 Intera 1.5T MRI machines due to potential adhesive failure in the Quadrature Body Coil seal, which may create sharp edges that could cause skin injuries or hair entanglement during patient scanning.

    Product
    Intera 1.5T Omni/Stellar, Model Number: 781104;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1782-2025·2025-05-21

    MRI Coil Seal Failure Creates Risk of Patient Skin Injury

    Philips MRI equipment may have a loose Quadrature Body Coil seal that creates sharp edges, risking patient skin lacerations and tissue injury. The seal adhesive can fail during scanning procedures.

    Product
    SmartPath to dStream for 1.5T, Model Number: 782146;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1783-2025·2025-05-21

    Philips MRI Machine Coil Seal May Develop Sharp Edges

    Philips SmartPath MRI equipment may develop a failing coil seal that creates sharp edges, potentially causing skin injuries and lacerations to patients during scanning.

    Product
    SmartPath to dStream for 3.0T, Model Number: 782145;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·25250·2025-05-08

    Maril Brand Scented Candles recalled due to laceration and fire hazards

    DEMDACO is recalling about 3,000 Maril Brand Scented Candles because the glass container can crack or break while burning, posing laceration and fire hazards. Three incidents of breaking have been reported with no injuries.

    Product
    Maril Brand Scented Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25214·2025-04-03

    Vivitar Blender Bottles Recalled by Sakar for Laceration Hazard

    Sakar International is recalling about 199,000 Vivitar Blender Bottles sold at Target because the blades can continue operating when the bottle is removed from the base. No injuries have been reported.

    Product
    Vivitar Blender Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25199·2025-03-27

    APOTHEKE Pumpkin Ginger Scented Candles Recalled for Fire and Burn Hazards

    APOTHEKE's Pumpkin Ginger 3-wick candles can overheat and break their glass containers, posing fire and burn hazards. About 640 units were sold at Crate & Barrel from June 2024 through January 2025.

    Product
    APOTHEKE's Pumpkin Ginger 3-Wick Scented Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25191·2025-03-20

    Bella Pro Series and Cooks espresso machines recalled due to burn and laceration hazards

    Sensio recalls about 12,300 Bella Pro Series and Cooks Steam Espresso machines because the brew cup handle can eject forcefully, shattering the carafe. Eight of 18 ejection reports involved burn and laceration injuries.

    Product
    Bella Pro Series and Cooks Steam Espresso machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide