Burn hazard recalls
Federal recalls citing a burn hazard.
- Past 12 months
- 153
- Past 90 days
- 28
- Past 30 days
- 7
- Past 7 days
- 3
Recall volume — past 12 months
per monthSeverity class
past 12 monthsWhere it shows up
top product categories- Consumer99
- Device54
- Baby38
- Appliance18
- Electronics14
- Apparel13
- 2026-02-05CPSCLittle CowStop using Little Cow Company candles
Little Cow Company's 9 oz soy candles in glass jars can crack or break during normal use, creating a risk of fire, burns, and cuts from broken glass. Two jars have broken so far, though no injuries have been reported yet.
- 2026-02-04CPSCMameixStop using Scepter B62 fuel containers
Scepter B62 fuel containers lack required safety devices to prevent flash fires and have non-child-resistant spouts that can cause burns or poisoning. These red containers with yellow spouts were sold online from August 2024 through May 2025.
- 2026-01-28FDA-DeviceMedlineClass IStop using Medline homecare bed hand control
Medline Industries has recalled certain Full Electric Low Lightweight Homecare Beds (model MDR107003LO) because the hand control pendant and its wires can overheat and catch fire in rare situations—such as when the bed is overloaded, blocked, or has jammed parts. The company has received 58 reports of the pendant sparking, burning, melting, smoking, or catching fire.
- 2026-01-28FDA-DeviceMedlineClass IStop using Medline Full Electric Lightweight Homecare Bed
The hand control pendant on Medline Full Electric Lightweight Homecare Beds (model MDR107003L) can overheat and catch fire in rare cases, especially if the bed is overloaded, blocked, or has jammed parts. Medline has received 58 reports of the pendant sparking, burning, melting, or smoking.
- 2026-01-28FDA-DeviceMedlineClass IStop using Medline homecare bed hand pendant
Medline's Full Electric Low Basic Homecare Bed (model MDR107003ELO) has a hand control pendant that may overheat and catch fire in rare cases—such as when the bed is overloaded, blocked from moving, or has jammed parts. Medline has received 58 reports of the pendant sparking, burning, melting, smoking, or catching fire. No injuries have been reported.
- 2026-01-28FDA-DeviceMedlineClass IStop using Medline Full Electric Basic Homecare Bed
Medline Industries is recalling certain Full Electric Basic Homecare Beds because the hand control pendant and cord may overheat and catch fire in rare situations—such as when the bed is overloaded, blocked, or has jammed parts. The company has received 58 reports of the pendant sparking, burning, melting, or smoking.
- 2026-01-28FDA-DeviceMedlineClass IStop using Medline MDR107002L homecare bed
Medline's Semi Electric Lightweight Homecare Bed (model MDR107002L) has a potential fire hazard in the hand control pendant and wires. In rare cases—such as when the bed is overloaded, blocked, or jammed—the pendant may overheat and spark, burn, melt, or catch fire. Medline has received 58 complaints of pendant sparking, burning, melting, smoking, or fire.
- 2026-01-28FDA-DeviceMedlineClass IStop using Medline homecare bed hand pendant
Medline's semi-electric homecare beds have hand control pendants that may overheat and catch fire in rare cases—for example, if the bed is overloaded, blocked, or jammed. The company has received 58 reports of the pendant sparking, burning, melting, or smoking.
- 2026-01-22CPSCXiyudeStop using Topkay torch lighters immediately
Topkay torch lighters sold on Amazon lack required child-resistant safety features, creating a risk of serious burns or fire. About 7,500 black two-packs labeled "Honest" were sold between September and October 2025.
- 2026-01-21FDA-DeviceMedlineClass IIMedline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE, REF CDS980754T; 2) GYN LAP HYSTERECTOMY CDS, REF CDS982662Q; 3) DAVINCI HYSTERECTOMY CDS, REF CDS985344F; 4) LAVH, REF DYNJQ9041R; 5) LAPAROSCOPIC HYSTERECTOMY, REF DYNJ900244I; 6) ROBOTIC LAVH, REF DYNJ901281I; 7) LAVH-LF, REF DYNJ901829T; 8) LEX LAP HYST, REF DYNJ902030J; 9) LITHOTOMY-SLINGS-LF, REF DYNJ905274D; 10) GYN LAPAROSCOPY, REF DYNJ905485J; 11) ROBOTIC HYSTERECTOMY, REF DYNJ906380C; 12)
Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.
- 2026-01-21FDA-DeviceMedlineClass IIStop using affected Medline surgical kits
Medline medical procedure convenience kits containing Stryker's Strykeflow 2 Suction Irrigators have a design flaw that allows irrigation solution to leak into the handpiece and battery pack during use. Some devices have leaked fluid or emitted vaporized saline that may resemble smoke during procedures.
- 2026-01-21FDA-DeviceMedlineClass IIStop using affected Medline laparoscopy kits
Medline medical procedure kits containing Stryker Strykeflow 2 Suction Irrigators may leak or emit vaporized saline during surgery due to a 2024 design change. The irrigation solution can travel into the handpiece and battery pack, potentially causing device malfunction or creating a smoke-like vapor in the surgical field.
- 2026-01-21FDA-DeviceMedlineClass IIStop using affected Medline robotic surgery kits
Medline medical procedure kits containing Stryker Strykeflow 2 Suction Irrigators have a design flaw that allows irrigation fluid to leak into the handpiece and battery pack during use. Some devices have leaked or released vaporized saline that may resemble smoke. This affects specific thoracic and cardiac robotic surgery kits distributed nationwide.
- 2026-01-21FDA-DeviceRepligenClass IIStop using Repligen MAVERICK Spectrometer
Repligen is recalling the MAVERICK Measurement Module Spectrometer due to cable connection defects that can cause two problems: the laser output may increase to unsafe levels, or the laser may fire unexpectedly during normal operation. A loose or poorly crimped cable under stress can trigger these faults. No injuries have been reported.
- 2026-01-15CPSCShangYu North Electron ManufactureStop using recalled Frigidaire minifridges immediately
Frigidaire-brand minifridges sold at Target can overheat and catch fire due to faulty electrical components. Curtis International has received six reports of fires in the EFMIS121 model, with property damage. The recall now includes about 330,000 additional units across five model numbers.
- 2026-01-15CPSCMorgan LaneStop using Morgan Lane Asher Pajamas immediately
Morgan Lane Asher Pajama Sets (Style 816TR in Petal, sizes 2T–14) fail to meet federal flammability standards for children's sleepwear and pose a serious burn hazard. These cotton pajamas with tiny rose prints were sold online from March 2024 through May 2025.
- 2026-01-15CPSCEnergizerStop using Energizer rechargeable lanterns immediately
Energizer is recalling about 4,100 Large Power Indicator Lanterns (model BGAAL9) with June 2024 date codes because the lithium-ion batteries can overheat and cause burns. One overheating incident has been reported, though no injuries so far.
- 2026-01-08CPSCPress Play ProductsStop using Isla Rae wireless chargers
Isla Rae magnetic wireless chargers can overheat and explode during use, creating a fire and burn risk. About 13,200 units were sold at T.J. Maxx and Marshalls stores between June 2024 and November 2025. No injuries have been reported so far.
- 2026-01-08CPSCMarcus AdlerStop using Julie and Judah pajamas and shorts
Marcus Adler Glove Co. is recalling Julie and Judah brand pajama pants and shorts because they don't meet federal flammability standards for children's sleepwear. These garments could catch fire more easily than safe sleepwear, risking burn injuries to children.
- 2025-12-18CPSCJuyuanStop using ANNQUAN power strips immediately
ANNQUAN power strips (models EX-D112-05 and EX-D106-25) lack proper safety protection and can overheat and catch fire if overloaded. Seven units have blown fuses. The fire risk can cause serious injury or death from burns and smoke.
- 2025-12-17FDA-DevicePhilipsClass IICheck your Philips Azurion 7 M20 X-ray system
Between July 2024 and June 2025, some Philips Azurion R3.0 fluoroscopic X-ray systems (model 722234) were shipped without a required safety spacer. This spacer ensures the X-ray tube maintains a safe distance from patients during standard fluoroscopy procedures, as required by FDA regulations.
- 2025-12-11CPSCVevorSanven Technology Recalls VEVOR Steamers Due to Risk of Serious Injury from Burn Hazard
The steamers can leak or spit hot water, posing a risk of serious burn injury to users and bystanders. The water tank cap can also leak or detach during use, exposing users to hot water.
- 2025-12-05CPSCSegmartINIU Recalls Power Banks Due to Fire and Burn Hazards; Sold on Amazon
The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers.
- 2025-12-03FDA-DeviceDJOClass IICold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02
The IFU (Information for Use) on the wrap instructs the user to heat the hot and cold compression wrap in the microwave for 3 minutes, which may cause the wrap to leak or break at the seams and/or reach temperatures capable of causing a second degree burn.
- 2025-12-03FDA-DevicePivotal Health SolutionsClass IIQuantum Intersegmental Table, Model/Catalog Number: AMQ400H; heated massage table
The heat function may become damaged over time due to patients pressing on the areas with heat function components. Damage to components can lead to overheating which can lead to smoldering and melting of the vinyl cushion.
- 2025-12-03FDA-DevicePivotal Health SolutionsClass IIQuantum Intersegmental Table, Model/Catalog Number: Q400; heated massage table
The heat function may become damaged over time due to patients pressing on the areas with heat function components. Damage to components can lead to overheating which can lead to smoldering and melting of the vinyl cushion.
- 2025-11-26FDA-DeviceMedlineClass IIMEDLINE convenience kits labeled as: 1) NEURO CRANIOTOMY CDS #36-RF, REF CDS780119V; 2) BASIC BACK CDS, REF CDS780147N; 3) INSTRUMENTED BACK CDS, REF CDS780148R; 4) NEURO-LAMI CDS, REF CDS780208I; 5) TOTAL HIP, REF CDS920027Y; 6) TOTAL KNEE, REF CDS940072Y; 7) TOTAL KNEE REPLACEMENT CDS, REF CDS940823AB; 8) TOTAL HIP CDS, REF CDS940843AA; 9) TOTAL HIP CDS, REF CDS940963Y; 10) SHOULDER CDS, REF CDS941065L; 11) LAMINECTOMY CDS-LF, REF CDS981923X; 12) TOTAL KNEE CDS, REF CD
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker Instruments has expanded the scope of their recall of SafeAir Smoke Evacuation Pencils previously initiated in October 2024, adding an additional 47 lots to the scope of the recall. The initial recall was due to the potential for product to activate without manual input when plugged into a power source or remain active after buttons are released.
- 2025-11-26FDA-DeviceMedlineClass IIMEDLINE convenience kits labeled as: GP-LEEP PACK-LF, REF PHS396969004F
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker Instruments has expanded the scope of their recall of SafeAir Smoke Evacuation Pencils previously initiated in October 2024, adding an additional 47 lots to the scope of the recall. The initial recall was due to the potential for product to activate without manual input when plugged into a power source or remain active after buttons are released.
- 2025-11-26FDA-DeviceMedlineClass IIMEDLINE convenience kits labeled as: 1) GYN LAPAROTOMY HARPER PACK-LF, REF DYNJ0160684F; 2) MAJOR LITHOTOMY PACK-LF, REF DYNJ0425778O; 3) MINOR VAGINAL #76-RF, REF DYNJ27434R; 4) ABDOMINAL HYST PACK, REF DYNJ44848M; 5) DA VINCI HYSTERECTOMY, REF DYNJ44863Q; 6) VAGINAL HYSTERECTOMY PACK, REF DYNJ44900P; 7) URO GYN, REF DYNJ50047G; 8) ISS VAG HYST PACK, REF DYNJ50315F; 9) PK MAJOR GYN ST MICHAEL C, REF DYNJ60554B; 10) VAGINAL HYSTERECTOMY PACK, REF DYNJ67194B; 11) LAVH, REF
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker Instruments has expanded the scope of their recall of SafeAir Smoke Evacuation Pencils previously initiated in October 2024, adding an additional 47 lots to the scope of the recall. The initial recall was due to the potential for product to activate without manual input when plugged into a power source or remain active after buttons are released.
- 2025-11-26FDA-DeviceMedlineClass IIMEDLINE convenience kits labeled as: 1) C-SECTION OR 30 CDS, REF CDS820075W; 2) C-SECTION, REF CDS984261J; 3) C-SECTION CDS, REF CDS985282F; 4) C-SECTION PACK, REF DYNJ02577D; 5) C-SECTION PACK-LF, REF DYNJ0536924U; 6) C-SECTION PACK-LF, REF DYNJ0551169V; 7) C-SECTION PACK-LF, REF DYNJ0551409P; 8) C-SECTION PACK-LF, REF DYNJ07836R; 9) C-SECTION, REF DYNJ14103C; 10) C-SECTION PACK, REF DYNJ19417R; 11) C-SECTION PACK-LF, REF DYNJ33059B; 12) C-SECTION PACK SC-LF, REF DYNJ38
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker Instruments has expanded the scope of their recall of SafeAir Smoke Evacuation Pencils previously initiated in October 2024, adding an additional 47 lots to the scope of the recall. The initial recall was due to the potential for product to activate without manual input when plugged into a power source or remain active after buttons are released.
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