fire hazard Recalls

250 recalls tagged with “fire hazard”.

Recalled Condor HMS Triple Locking Carabiner
HIGH
CPSC

OCUN NA Recalls Condor HMS Triple Carabiners Over Fall Hazard (2026)

OCUN NA recalled Condor HMS Triple Carabiners sold online and through climbing retailers after the gate may fail to close automatically. The carabiner features an independent internal wire gate and a triple locking action. Stop using the recalled carabiner immediately and contact OCUN NA for a free replacement.

OCUN NA
The carabiner's
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Recalled DIY Sauna Heater Kit (shown assembled in sauna)
HIGH
CPSC

DIY Cold Plunge Sauna Heater Kit Recalled for Fire Hazard in 2026

DIY Cold Plunge recalled its Sauna Heater Kit sold online after electrical conductors can overheat and cause a fire. The defect involves overheating electrical conductors in the kit's wiring. Stop using the kit now and register for a full refund at the recall page.

DIY Cold Plunge
Electrical conductors
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Recalled gas connector with label
HIGH
CPSC

DuraTrac Recalls Stainless Steel Gas Connectors for Fire Hazard (2026)

DuraTrac recalled stainless steel gas connectors sold at Ace Hardware, Blake's Inc., and Merritt’s Hardware from May 2025 through November 2025. The recall cites a manufacturing defect that could cause a gas leak and a fire hazard. Consumers should stop using the recalled connectors immediately and contact DuraTrac for a full refund.

DuraTrac
The recalled
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Recalled Nomic Ice Climbing Axe
HIGH
CPSC

Petzl America Recalls Nomic and Ergonomic Ice Climbing Axes Over Fall Hazard (2026)

Petzl America recalls Nomic and Ergonomic ice climbing axes due to a shaft break risk that could cause a fatal fall. The recall involves specific serial ranges across two models and targets accessories sold through specialty retailers and online shops. Consumers should stop using the axes and pursue a free repair kit from Petzl America.

Petzl America
The ice
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Recalled Vive Health Compact Bed Rail (model number LVA2009SLV)
HIGH
CPSC

Vive Health Bed Rails Recall Expands as Entrapment, Asphyxiation Risk Causes Two Deaths

Vive Health recalled adult portable bed rails after two deaths were linked to entrapment and asphyxiation. The recall covers the Compact Bed Rail model LVA2009SLV, Bed Rail Collection V model LVA2097SLV, and LVA1024 units purchased on or before August 21, 2023. A prior recall covered LVA1024 units purchased after that date. Consumers must stop using these rails and seek a full refund from Vive.

Vive Health
When the
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Food & Beverages
HIGH
FDA FOOD

Connecticut Crab Company Crab Cakes Recalled for Temperature Abuse Risk, 39 Boxes Affected

Connecticut Crab Company LLC recalls 39 boxes of crab cakes sold to food service due to potential temperature abuse that could enable Clostridium botulinum growth. The recall notice is active as of April 15, 2026. Consumers who purchased these products should not consume them and should seek refund or replacement information from the company.

Connecticut Crab Company
May be
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Health & Personal Care
HIGH
FDA DRUG

Fagron Compounding Services Vancomycin HCI Recall: 34,260 Bags with Break-Off-Part Risk (2026)

Fagron Compounding Services recalled 34,260 bags of Vancomycin HCI Injection across the United States. The recall cites lack of sterility assurance and a blue Break-Off-Part that could detach from the administration port. Healthcare providers and patients should stop using the product immediately and follow manufacturer guidance.

Fagron Compounding Services
Lack of
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Recalled Frigidaire Range Model PCFG3080AF
HIGH
CPSC

Electrolux Group Recalls Frigidaire Gas Ranges for Burn Hazard (2026)

Electrolux Group recalled Frigidaire gas ranges sold nationwide through retailers after a burn hazard was identified. The bake burner can ignite with delay, creating a burn risk. Stop using the recalled ovens immediately and contact Electrolux for a free in-home bake burner repair; cooktops remain usable.

Electrolux Consumer Products, Inc., of Charlotte, North Carolina
The ovens
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Health & Personal Care
HIGH
FDA DRUG

Teva Octreotide Acetate Injectable Suspension Recall 21,930 Cartons Over Sterility Risk (2026)

Teva Pharmaceuticals recalled 21,930 cartons of Octreotide Acetate for Injectable Suspension distributed nationwide in the United States. The recall stems from lack of assurance of sterility identified during an FDA inspection at the contract manufacturer. Healthcare providers and patients should stop using this product immediately and contact Teva or a physician for guidance.

OCTREOTIDE ACETATE
Lack of
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Health & Personal Care
HIGH
FDA DRUG

Fresenius Kabi Saline Solution Recalled for Lack of Sterility Assurance (2026)

Fresenius Kabi USA recalled saline injections distributed nationwide, including Alaska and Puerto Rico. The action covers multiple batch numbers with sterility concerns. Healthcare providers and patients should stop using the product immediately and follow official guidance for replacement options.

SODIUM CHLORIDE
Lack of
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