74 recalls tagged with “battery powered”.
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.
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
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.
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
ShymeryDirect LED Lights are recalled. The recall was issued on April 9, 2026. The recall involves 24 LED lights containing two CR2032 lithium coin batteries each. Packaging code X0037GYJYX is shown on the product. Consumers should stop using the lights and contact Shymeryrecall0402@outlook.com for a full refund.
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.
Gavoyeat recalled 50-ring Halloween Light-Up Rings sold on Amazon by CSZWEICD on April 2, 2026. The recall cites a battery ingestion hazard from an accessible button cell battery in the ring’s housing. Stop using the recalled rings and return them for a full refund by emailing recalledgavoyeat@yeah.net.
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.
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.
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.
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
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.
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.
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.
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 is recalling 798 Azurion 3 M15 systems worldwide, including 42 units in the United States. The wired foot switch may fail to initiate X-ray imaging or fail to produce consistent imaging. Healthcare providers should stop using the affected devices and follow recall instructions issued by Philips.
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 Respironics recalled 113,717 Trilogy Evo Universal home-use ventilators sold by multiple retailers after alarms may fail to trigger. The obstruction alarm may not trigger within the required timeframe, delaying warning by up to four breaths. Patients should stop using the device and follow the manufacturer’s recall instructions or contact their healthcare provider for guidance.
Philips Respironics recalled 113,717 Trilogy Evo Universal ventilators worldwide on March 2, 2026. The recall cites a condition where using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the delivered tidal volume. Patients and caregivers should stop using the device immediately and contact Philips Respironics or their healthcare provider for instructions.
SumDirect recalled LED mini lights on February 26, 2026, due to a serious ingestion risk from button cell batteries. The recall affects products that are easily accessible to children and lack required safety warnings. Consumers should stop using the lights immediately and seek a refund.