battery powered Recalls

83 recalls tagged with “battery powered”.

Recalled Wybot S1 (Top)
HIGH
CPSC

Wybotics Recalls Osprey 700 Max and S1 Robotic Pool Vacuums for Burn and Fire Hazards (2026)

Wybotics is recalling specific Osprey 700 Max and S1 robotic pool vacuums sold through retailers after reports that the lithium-ion battery can overheat, creating a burn and fire hazard. The recall covers Osprey 700 Max models WY3312MAX and WY100MAX and S1 WY200, with serial numbers WY100M230117XXXX, WY100M230127XXXX, WY100M230130XXXX, WY100M230318XXXX, WY200-230328XXXX and W200**230330XXXX. The U

Wybotics, Co. Ltd. of Tianjin, Chin
The lithium-ion
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Recalled VEEKTOMX Mini Power Bank (White)
HIGH
CPSC

VEEKTOMX VT103 Mini Power Bank Recall 2026 for Fire Hazard

Shenzhen Baihang recalled VEEKTOMX VT103 Mini Power Banks sold on Amazon. The recalled devices contain a lithium-ion battery that can overheat and ignite. Consumers should stop using the recalled power banks immediately and contact Shenzhen Baihang or Veektomx for a free replacement.

Shenzhen Baihang
The lithium-ion
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Recalled Besslly Halloween Pumpkin Carving Kit
CRITICAL
CPSC

Besslly Halloween Pumpkin Carving Kit CHD-014-2 Recalled for Battery Ingestion Risk (2026)

Besslly recalled its CHD-014-2 Halloween Pumpkin Carving Kit sold on Amazon after the tea lights’ button-cell batteries pose an ingestion risk. The recall involves five tea lights with 15 button batteries and a set of carving tools, emoticon stickers, a handbag, and gloves, and it lacks the Reese’s Law warnings. Stop using the recalled kit now and email tingjmng@outlook.com to receive a fullrefund

Halloween Pumpkin Carving Kits
The recalled
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Recalled Happiness Light LED Lights
HIGH
CPSC

Happiness Light LED Lights Recalled for Battery Ingestion Risk (2026)

Happiness Light recalled LED lights sold on Amazon after determining two CR2032 lithium coin batteries inside the unit could be accessed by children. Each light contains two coin batteries. Consumers should stop using the recalled lights and request a full refund by emailing usa@happinesslight.com.

LED Lights
The recalled
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Vehicles & Parts
HIGH
NHTSA

Mercedes-Benz Recalls EQS SUV 580 Over Battery Management Software

Mercedes-Benz USA recalled the 2025 EQS SUV 580 4MATIC on April 5, 2026. The recall affects vehicles due to battery management software issues that can cause a sudden loss of drive power. This malfunction increases the risk of a crash, prompting immediate action by the company.

Mercedes-Benz USA, LLC
A sudden
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Recalled Coluans Christmas Light-Up Rings Party Favors
HIGH
CPSC

Coluans Christmas Light-Up Rings Recalled for Battery Ingestion Risk (2026)

Coluans recalled Christmas Light-Up Rings sold on Amazon by BUDI Official. The recall centers on a battery ingestion hazard from three preinstalled button cell batteries visible through the ring’s clear casing. Stop using the rings immediately and return them for a full refund by emailing BUDIrecall@outlook.com with a photo of the disposed product.

Coluans Christmas Light-Up Rings
The recalled
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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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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 Built LUUM LED Tumbler - FESTIVE FOREST
HIGH
CPSC

Lifetime Brands Recalls BUILT LUUM Light Up Tumblers for Choking and Battery Ingestion Hazards (2026

Lifetime Brands recalls BUILT LUUM Light Up Tumblers sold at multiple retailers. The recall covers 16 oz and 18 oz plastic cups with a lid and straw that contain a bottom LED light powered by a button cell battery. Labels on the underside or hangtags show the theme and item numbers with UPCs. Stop using these tumblers immediately and seek a full refund by contacting Lifetime Brands.

Lifetime Brands
The recalled
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Health & Personal Care
HIGH
FDA DRUG

Teva Octreotide Acetate Injectable Suspension Recall 19,869 Cartons Nationwide (2026)

Teva Pharmaceuticals USA recalled 19,869 cartons of Octreotide Acetate for Injectable Suspension nationwide in the United States after FDA inspection flagged lack of assurance of sterility at the contract manufacturer. The FDA cited quality system deficiencies at Pharmathen International S.A. in Greece. Healthcare providers and patients should stop using the product immediately and contact Teva or

OCTREOTIDE ACETATE
Lack of
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Food & Beverages
HIGH
FDA FOOD

Nuts.com Espresso Malted Milk Balls Recalled for Undeclared Wheat and Soy (2026)

Nuts.com recalled 10,190 pounds of Espresso Malted Milk Balls distributed nationwide in the United States. The recall cites undeclared wheat and soy allergens from soy lecithin in the ingredient statement. Consumers who bought this product should not consume it and should contact Nuts.com for a refund or replacement via email.

Nuts.com
Undeclared Allergen
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Recalled Cubimana Pirate Ship Building Set box with model number (front)
HIGH
CPSC

Cubimana Island Storm Building Sets Recalled Over Battery Ingestion Risk

Cubimana recalled its Island Storm 3 In 1 Building Sets on March 5, 2026, due to a risk of serious injury or death from battery ingestion. The sets violate safety standards as they contain accessible button cell batteries. Consumers should stop using and return the product immediately for a full refund.

Cubimana Island Storm 3 In 1 Building Sets
T The
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Food & Beverages
HIGH
FDA FOOD

Ajinomoto Foods North America Recalls 3,059,808 Lbs Trader Joe's Fried Rice For Glass Contamination

Ajinomoto Foods North America recalls 3,059,808 pounds of Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed sold nationwide after glass fragments were found in the product. The glass pieces range from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat the product and should seek a refund or replacement. The recall number is H-0591-2026.

Ajinomoto Foods North America
Foreign objects
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Health & Personal Care
HIGH
FDA DRUG

K.C. Pharmaceuticals Sterile Eye Drops Recall 315,144 Bottles for Lack of Sterility (2026)

K.C. Pharmaceuticals recalled 315,144 sterile eye drop bottles distributed nationwide after lack of sterility. The products span several brands including GNP Eye Drops Redness and Dry Eye Relief, Leader Eye Drops Redness Relief, and Foster & Thrive Redness Relief Eye Drops. Consumers should stop using the products immediately and follow guidance from KC Pharmaceuticals or their healthcare provider

GNP Eye Drops Redness and Dry Eye Relief
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD10C X-ray System Recall for 15 Units Worldwide (2026)

Philips Medical Systems Nederland B.V. recalled 15 Allura Xper FD10C radiography systems worldwide, including 7 in the United States and 8 overseas. The devices may fail to initiate X-ray imaging or intermittently stop imaging when using the wired foot switch. Facilities should stop using the devices and await recall instructions from Philips.

Philips Medical Systems Nederland B.V.
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20/10 Recall Affects 85 Imaging Systems in 2026

Philips recalled 85 Allura Xper FD20/10 imaging systems distributed nationwide and internationally. The devices may fail to initiate X-ray imaging or do so intermittently when using the wired foot switch. Hospitals and clinicians should stop using the device and follow the manufacturer’s recall instructions.

PHILIPS MEDICAL SYSTEMS NEDERLAND
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Civco Medical Instruments Recalls 21 eTRAX Needle Sensors for Aurora Trackers (2026)

Civco Medical Instruments Co. recalled 21 eTRAX Needle Sensors for Aurora Trackers sold to healthcare providers in Ohio, Pennsylvania and Washington. The devices have an inspection and programming error that can cause the needle tip position to be misidentified on the user interface. Clinicians should stop using the devices immediately and follow recall instructions from Civco.

Civco Medical Instruments Co.
There was
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Tag Statistics

Total Recalls
83

Related Tags

burn riskfire hazardelectrical hazardlithium batteryimmediate actionstop use immediatelyreturn for refundreplacement availablecpsc regulatedoutdoorpoisoning riskholiday product