immediate action Recalls

2,679 recalls tagged with “immediate action”.

Vehicles & Parts
HIGH
NHTSA

GM Recalls 2024 Silverado EV and 2024-2025 Sierra EV for Rear Seat Belt Anchorage Issue

General Motors recalls 2024 Chevrolet Silverado EV and 2024-2025 GMC Sierra EV pickups for a rear center seat belt anchorage bolt that may not have been tightened. The bolt may fail to restrain an occupant in a crash. Vehicles are in dealer inventory and no owner letters will be mailed. Contact GM at 1-888-988-7267 or Chevrolet at 1-800-222-1020 for service.

General Motors
An improperly
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Food & Beverages
HIGH
FDA FOOD

HEYTEA USA Coconut Drink 1 Recalled Over Undeclared Milk in 12,677 Cartons (2026)

HEYTEA USA INC recalls 12,677 cartons of Coconut Drink 1 sold for catering establishments in multiple states after undeclared milk was found. The product contains milk not listed on the label. Consumers should not consume the product and contact HEYTEA USA INC for refund or replacement by email.

HEYTEA USA
Product contains
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Health & Personal Care
HIGH
FDA DRUG

Biocon Pharma Prazosin Hydrochloride 1mg 100-Count Capsules Recalled for Nitrosamine Impurity (2026)

Biocon Pharma Inc. recalled 88,008 bottles of Prazosin Hydrochloride capsules, 1 mg, 100-count bottles, nationwide in the United States. A cGMP deviation detected N-nitroso-prazosin impurity C above acceptable limits. Consumers and healthcare providers should stop using this product immediately and contact Appco Pharma LLC or a healthcare provider for guidance.

Biocon Pharma
cGMP deviation:
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Health & Personal Care
HIGH
FDA DRUG

Biocon Pharma Prazosin Hydrochloride 5mg Recall 28,157 Bottles Over Nitrosamine Impurity (2026)

Biocon Pharma Inc. recalled 28,157 bottles of PRAZOSIN HYDROCHLORIDE capsules, distributed nationwide in the USA. The recall cites cGMP deviation due to detection of N-nitroso-prazosin impurity C above acceptable limits. Stop using the product immediately and contact Appco Pharma LLC or your healthcare provider for guidance.

Prazosin Hydrochloride
cGMP deviation:
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Health & Personal Care
HIGH
FDA DRUG

Biocon Prazosin Hydrochloride 2 mg Capsules Recalled for Nitrosamine Impurity (58,896 bottles, 2026)

Biocon Pharma Inc. recalled 58,896 bottles of Prazosin Hydrochloride Capsules, USP, 2 mg, 100-count bottle. The product was distributed nationwide in the USA and manufactured by Appco Pharma LLC. A cGMP deviation detected N-nitroso-prazosin impurity C above acceptable limits. Consumers and healthcare providers should stop using this product immediately and contact Appco Pharma LLC or their health‑

Prazosin Hydrochloride
cGMP deviation:
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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 AirClub Convertible Bassinet – Front View light grey
MEDIUM
CPSC

AirClub Recalling convertibles Bassinets for Bedside Sleepers Over Fall Hazard (2026)

AirClub recalled convertible bassinets that convert into bedside sleepers due to a hazardous attachment mechanism. The recall affects models labeled QX-831. The defect creates an opening between the bedside sleeper and mattress, posing a risk of serious injury or death to infants. Stop using the product immediately and contact AirClub for a replacement attachment mechanism.

AirClub
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 Sunnyyes LED Lights with remote controls
HIGH
CPSC

Sunnyyes LED Mini Lights Recalled for Battery Ingestion Risk, Despite Reese’s Law Violations

Sunnyyes LED mini lights are recalled after reports of serious injury risk from accessible coin batteries. The recall covers Sunnyyes branded lights sold nationwide. The hazard stems from lithium coin batteries accessible to children, plus a loose remote-control battery screw and missing parental warnings. Stop using the product and contact Sunnyyes for a full refund.

Sunnyyes LED Mini Lights
The recalled
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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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Health & Personal Care
HIGH
FDA DRUG

Amneal TRAMADOL HYDROCHLORIDE 50 mg Recall 29,542 Bottles Over Impurity (2026)

Amneal Pharmaceuticals is recalling 29,542 bottles of TRAMADOL HYDROCHLORIDE tablets distributed nationwide in the United States. The recall cites a failed impurity specification for N-nitroso-desmethyl-tramadol (NDSRI) at the 24‑month stability interval. Consumers and healthcare providers should stop using the product immediately and contact Amneal for guidance.

TRAMADOL HYDROCHLORIDE
Failed Impurities/Degradation
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Recalled Wagner Model 905e Auto Steamer, pictured with included accessories
HIGH
CPSC

Wagner Spray Tech Recalls 900-Series Power Steamers Over Burn Hazard (2026)

Wagner Spray Tech recalls 900 Series power steamers, including the 905e Auto Steamer, 915e On-Demand Power Steamer, and 925e Steam Machine Elite Steamer. The recall cites a burn hazard from an overheating hose and hot-water expulsion from the nozzle. Consumers should stop using the recalled steamers immediately and contact Wagner for a free repair kit.

Wagner Spray Tech
The attached
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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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