fire hazard Recalls

250 recalls tagged with “fire hazard”.

Vehicles & Parts
HIGH
NHTSA

Chevrolet Corvette 2025 Recall for Fuel System Fire Risk After Refueling Spill

Chevrolet Corvette owners are being notified by General Motors dealers to fix a fuel-spill risk in 2023–2026 Corvette models. During refueling, excess fuel may spill into the vehicle fuel-filler pocket and reach an ignition source, increasing fire risk. Dealers will install a shield at no charge. Letters were mailed Sept. 10, 2025. Owners should contact Chevrolet customer service at 1-800-222-1020

Chevrolet
A fuel
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific L221 PROPONENT DR EL Pacemaker Recalled for Safety Software Issue (2025)

Boston Scientific is recalling 3,592 pacemakers sold worldwide through hospitals and clinics in 2025. A software feature intended to enhance Safety Architecture may fail to initiate Safety Mode in ambulatory settings due to high battery impedance. Patients and healthcare providers should stop using these devices immediately and follow the recall instructions.

Boston Scientific
Software to
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Health & Personal Care
HIGH
FDA DEVICE

Aesculap AG Recalls ELAN 4 Fixed Duraguard Long Mislabeling Devices (GB943R)

Aesculap AG recalls the ELAN 4 Fixed Duraguard Long device, Model GB943R, after mislabeling errors were discovered. The U.S. distribution reached Missouri with international distribution to multiple countries. Healthcare providers should stop using the device immediately per manufacturer instructions.

Aesculap AG
Mislabeling. The
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Food & Beverages
HIGH
FDA FOOD

ADMIRAL OF THE FLEET, PORTICO SEAFOOD CLASSIC Breaded Shrimp Recalled Over Cs-137 Contamination (120

ADMIRAL OF THE FLEET and PORTICO SEAFOOD CLASSIC Cleantail Breaded Butterfly Shrimp is recalled by TAMPA MAID FOODS, LLC after the FDA identified Cesium-137 contamination. The recall covers 1,200 cases distributed to multiple states. Consumers should not consume the product and should contact TAMPA MAID FOODS for refund or replacement.

ADMIRAL OF THE FLEET
Product may
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Recalled LED module
HIGH
CPSC

Viewrail Recalls LED Control Module for Floating Stairs Over Fire Hazard

Viewrail recalls the electronic LED module E2-WR used with floating stairs and rails after a fire hazard was identified. The recall covers modules located inside the metal stringer tube at the back of the stairs. The recall was announced by the CPSC on 2025-08-14. Consumers should stop using the module and contact Viewrail for a replacement or refund.

Viewrail
The LED
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Health & Personal Care
HIGH
FDA DEVICE

Penner Patient Care Bathing Spa Devices Recall for Missing Unique Device Identifier (Z-1500-2026)

Penner Patient Care recalled 643 devices nationwide after the FDA flagged missing unique device identifiers. The recall affects a broad range of Penner Pacific Bathing Spa models. The device lacks a unique device identifier, posing regulatory and traceability concerns. Stop using the device and follow recall instructions from Penner Patient Care or a healthcare provider.

Penner Patient Care
The device
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Health & Personal Care
HIGH
FDA DEVICE

Max Mobility/Permobil Recalls 8,413 Smart Drive MX2+ SpeedControl Dials (2025)

Max Mobility LLC recalls 8,413 Smart Drive MX2+ SpeedControl Dials used with the SmartDrive MX2+ Wheelchair Power Assist. A faulty electrical connection between the dial and the motor can cause loss of control. Stop using the device immediately and follow recall letters for instructions.

Max Mobility
Due to
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Recalled La Ligne Enfant Bonne Nuit Pajamas in Navy with White Trim
HIGH
CPSC

La Ligne Enfant Bonne Nuit Pajamas Recalled for Burn Hazard in 2025

La Ligne recalls Enfant Bonne Nuit children’s pajamas after a burn hazard was identified. The recall covers La Ligne by La Ligne Enfant Bonne Nuit two-piece sets sold in various colors. Consumers should stop using the pajamas and pursue a full refund or store credit.

La Ligne
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific NephroMax Kit Recall Covers 458 Units Over Foreign Material Migration Risk

Boston Scientific Corp. recalls 458 NephroMax Kit units using Encore 26 Inflation Devices after an internal review found foreign material particles could migrate from the inflation device into balloon dilatation catheters. The recall affects UPNs M0062101180 and M0062101600 worldwide. Healthcare providers should stop using the device immediately and follow manufacturer recall instructions.

Boston Scientific
The Encore
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Health & Personal Care
HIGH
FDA DEVICE

Wasatch Photonics Raman Spectrometers Recall Expanded for Laser Safety Risks (2025)

Wasatch Photonics recalled 192 Raman spectrometers in the United States after identifying two potential laser safety failure modes. Models 785-SR-ILP, 785-SR-ILC, 830-SR-ILP, 830-SR-ILC, and 785-ER-ILC are included. The defect could occur under excessive force or extreme continuous vibration. Stop using immediately and follow the manufacturer’s recall instructions.

WASATCH PHOTONICS
Two new
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Health & Personal Care
HIGH
FDA DRUG

Hospira Epinephrine Injection Vials Recalled for Lack of Sterility Assurance (2025)

Hospira recalls 49,620 vials of Epinephrine Injection, distributed nationwide in the United States. The recall, active since August 4, 2025, targets vials with NDC 0409-4933-05 and case NDC 0409-4933-10. The hazard is lack of assurance of sterility. Health professionals should stop using the product and contact Pfizer or a healthcare provider for guidance.

Epinephrine
Lack of
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Recalled Baby Loren Children's Joy Loungewear
HIGH
CPSC

Baby Loren Recalls 4 Morning Loungewear Styles for Burn Risk (2025)

Baby Loren recalls four Morning children’s 100% cotton loungewear dresses in 2025 for fire safety violations. The recall involves dresses with neck labels listing October 2022 or October 2023 and batch numbers ending in 3465, 3585, 3599 or 3569. Consumers should stop using the dresses and contact Baby Loren for a full refund.

Baby Loren
The recalled
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Recalled Amazon Basics Premium Foam Eurotop Mattress
HIGH
CPSC

Amazon Recalls Amazon Basics Premium Foam Eurotop Mattress for Fire Hazard (2025)

Amazon recalled Amazon Basics Premium Foam Eurotop Mattresses sold on Amazon. The nine-inch mattresses in twin, full, queen and king sizes were manufactured from 12/22/2022 through 05/16/2024 and violate the federal flammability standard, posing a fire hazard. Stop using the recalled mattress and contact Amazon for a full refund.

Amazon
The recalled
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Tag Statistics

Total Recalls
250

Related Tags

chemical hazardimmediate actionstop use immediatelyrepair availablereplacement availablereturn for refundnhtsa regulatedelectrical hazardsuffocation riskinfant producttoddler productadult product