stop use immediately Recalls

2,228 recalls tagged with “stop use immediately”.

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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Food & Beverages
HIGH
FDA FOOD

Zarlengo Italian Ice Recalls Chocolate Chocolate Chip Gelato Over Soy Lecithin Ingredient Mismatch (

Zarlengo Italian Ice recalls 1,333 units of Chocolate Chocolate Chip Gelato distributed in Illinois, Indiana and Texas after discovering a mismatch between ingredients and contains statements. Soy lecithin appears in the ingredients list but is not referenced in the contains statement. The recall is Class II with high hazard potential. Consumers should not consume the product and should seek a退款或替

Zarlengo Italian Ice
Soy Lecithin
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Recalled 4our Kiddies Plastic Tip Restraint
HIGH
CPSC

4our Kiddies Tip Restraint Kits Recalled Over Tip-Over Hazard in 2026

Fourour Kiddies recalled tip restraint kits after tests found plastic components could break, creating a tip-over risk. The recall affects kits used to secure furniture to walls. Consumers should stop using the recalled restraints and seek a stainless steel replacement from 4our Kiddies.

4our Kiddies
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 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

ARTIFICIAL TEARS Eye Drops Recalled for Sterility Concerns, 720 Bottles Distributed Nationwide (2026

Geri-Care eye drops recalled nationwide after lack of sterility assurance affects 720 bottles. The product, ARTIFICIAL TEARS with NDC 68788-7266-0, is manufactured by Preferred Pharmaceuticals, Inc. in Brooklyn, NY. The FDA recall class II points to a risk of contamination. Stop using immediately and contact a healthcare provider for guidance.

ARTIFICIAL TEARS
Lack of
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Tag Statistics

Total Recalls
2,228

Related Tags

chemical hazardpoisoning riskimmediate actionreturn for refundfda regulatedcpsc regulatednhtsa regulatedreplacement availableelectroniclithium batteryglassinfant product