immediate action Recalls

2,679 recalls tagged with “immediate action”.

Food & Beverages
HIGH
FDA FOOD

DEVI Cinnamon Powder Recall: 140 Packets in WA for Lead Contamination (2025)

DEVI brand Cinnamon Powder, imported and distributed by Homeneeds Inc. in Bellevue, WA, is recalled after FDA testing found lead at 2.92 mg/kg. The recall covers 7 cases and about 140 packets. Consumers should not consume the product and contact Homeneeds for a refund or replacement.

DEVI
Elevated levels
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Food & Beverages
HIGH
FDA FOOD

M.C.I. Foods Recalls 1,040 Cases of Ready-to-Eat Egg & Cheese Breakfast Burritos and Wraps (2025)

M.C.I. Foods recalled 1,040 cases of ready-to-eat Egg and Cheese Breakfast Burritos and Wraps sold to seven distributors nationwide for institutional use. A cooked egg ingredient used in the ready-to-eat products tested positive for Listeria monocytogenes. Consumers should not consume the product and should contact M.C.I. Foods for refund or replacement; notification will be by letter.

M.C.I. Foods
Cooked egg
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Recalled Wilteexs Bioethanol Fuel Bottle
HIGH
CPSC

Wilteexs Bioethanol Fuel Bottles Recall 2025 Over Flash-Fire Risk

Wilteexs recall 1-liter bioethanol fuel bottles imported by Wilteexs after safety-standard violations. The bottles lack flame mitigation devices and carry a false “Non Toxic” disclaimer. Consumers should stop using the recalled bottles and contact Wilteexs for a full refund.

Wilteexs
The ethanol
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Recalled VR Plus and VT Series Vesta Water Heaters
CRITICAL
CPSC

VESTA.DS Recalls VST Tankless Water Heaters for CO Poisoning Hazard (2025)

VESTA.DS recalled VST-brand residential tankless water heaters sold nationwide through retailers after the potential carbon monoxide poisoning hazard was identified. The exhaust duct can crack, letting gases escape into homes and potentially cause death or serious injury. Stop using the recalled water heater and contact VESTA.DS for a free repair; if you must continue using it, install working烟雾与一

VESTA.DS
The exhaust
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Recalled WLIVE Fabric 12-Drawer Dresser in Rustic Brown Wood Grain Print
HIGH
CPSC

WLIVE Fabric 12-Drawer Dressers Recalled for Tip-Over Risk (2025)

WLIVE recalled its Fabric 12-Drawer Dressers sold on Amazon after identifying a serious tip-over and entrapment hazard. The dressers are unstable if not anchored to the wall, violating the mandatory standard for clothing storage units under the STURDY Act. Consumers should stop using the recalled dressers immediately and contact WLIVE for a full refund.

WLIVE
The recalled
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Recalled E-Z-GO Valor PTV
HIGH
CPSC

Textron E-Z-GO Recalls Personal Transportation Vehicles Over Fuel Leak Fire Hazard (2025)

Textron E-Z-GO recalled certain personal transportation vehicles due to a fuel-line leak that can spark a fire. The recall covers RXV Freedom and Valor PTVs from model years 2020-2025 and TXT Freedom and Valor PTVs from model years 2020-2022. Dealers will inspect and replace the fuel line at no cost, and owners should stop using the vehicles until inspected.

Textron E-Z-GO
The recalled
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Food & Beverages
HIGH
FDA FOOD

M.C.I. Foods Recalls 330 Cases of Cheese and Egg with Green Salsa Breakfast Burrito Over Listeria (H

M.C.I. Foods recalled 330 cases of Cheese and Egg with Green Salsa Breakfast Burrito sold to seven distributors nationwide. The ready-to-eat burrito contains a cooked egg ingredient that tested positive for Listeria monocytogenes. Consumers should not eat the product and should contact M.C.I. Foods for refund or replacement by letter.

M.C.I. Foods
Cooked egg
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Recalled DR2A and DR2E Golf Cars
HIGH
CPSC

Yamaha Recalls 2017-2024 Golf Cars Over Brake Failure Crash Hazard (2025)

Yamaha recalled model year 2017-2024 DR2A and DR2E Personal Transportation Vehicles sold through Yamaha dealers nationwide from June 2018 through July 2025. The brake system may fail to engage, creating a crash hazard with potential for serious injury or death. Owners should stop using the recalled golf cars and contact an authorized Yamaha Golf Car dealer to arrange a free brake repair. Yamaha or

Yamaha
The recalled
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Recalled Yamaha Drive 2 J0D/J0E/J5C
HIGH
CPSC

Yamaha Recalls 2021-2025 Drive 2 Golf Cars for Crash Hazard With No Stop Lights

Yamaha recalls 2021-2025 Drive 2 PTV golf cars sold by Yamaha dealers nationwide between June 2020 and July 2025. The recalled golf cars lack stop lights, creating a crash hazard that could result in serious injury or death. Owners should stop using the recalled golf car immediately and contact an authorized Yamaha Golf Car dealer for a free installation of two stoplights.

Yamaha
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Recalls Bicarbonate Reagent Over High Result Risk

Beckman Coulter recalled 36,981 bicarbonate reagents on October 14, 2025. The reagent may produce falsely high bicarbonate results due to interference from Lactate Dehydrogenase. Healthcare providers and patients must stop using it immediately.

Beckman Coulter Ireland
Bicarbonate reagent
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Health & Personal Care
HIGH
FDA DEVICE

MRIMed Recalls Mobile Exam Light Battery Over Overheating Hazard

MRIMed recalled 314 batteries for the SL-110 Mobile Exam Light on October 13, 2025. The batteries can overheat while charging, melting internal components and producing smoke. This recall affects devices distributed in the U.S. and several countries worldwide.

MRIMed
Due to
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Health & Personal Care
HIGH
FDA DEVICE

DERMASENSOR DermaSensor 10101 Diagnostic Device Recalled for 9 of 343 Units (2025)

DermaSensor recalled 343 units of its DermaSensor 10101 diagnostic device distributed to medical practices across several states. The device may not meet specifications, producing incorrect results or delaying referrals for patients with suspicious skin lesions. Health care providers should stop using the device immediately and contact Dermasensor Inc for instructions.

DERMASENSOR
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Paragon 28 Phantom Fibula Nail Recall 2025 for 20 Units Nationwide

Paragon 28 recalled 20 Phantom Fibula Nails nationwide after finding out-of-spec thread depths. The defect may prevent the nail from mating properly with the mounting bolt. Surgery could be aborted if the implant cannot mate with instrumentation. Hospitals and surgeons should stop using the device immediately and follow recall instructions.

Paragon 28
Fibula nail
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Health & Personal Care
HIGH
FDA DRUG

470 Doctor D. Schwab Controlling Cream Tubes Recalled for CGMP Deviations

Doctor D. Schwab recalled 470 tubes of Controlling Cream after discovering CGMP deviations in production. The cream, which contains benzoyl peroxide, may not meet required safety standards. Consumers should stop using the product immediately and contact CA BOTANA for further guidance.

Doctor D. Schwab
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Sugared+Bronzed Tinted Mineral Sunscreen SPF 50 Recalled for CGMP Deviations (Class II)

Sugared+Bronzed recalled 2,090 tubes of tinted mineral sunscreen distributed to California, Colorado, Florida, Puerto Rico and Washington after CGMP deviations were found. The recall, initiated by CA BOTANA International, is active as of Dec 3, 2025. Consumers should stop using the product immediately and contact the distributor for guidance.

Sugared+Bronzed
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Gabapentin 100 mg Capsules Recalled by Major Pharmaceuticals in 2025, 100-Count Pack

Major Pharmaceuticals recalled Gabapentin capsules, 100 mg, 100-count, distributed nationwide in the United States. The recall stems from an out-of-spec highest unknown impurity found during stability testing. Healthcare providers and patients should stop using the product and contact The Harvard Drug Group LLC for guidance.

Gabapentin
Failed Impurities/Degradation
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