293 recalls tagged with “battery powered”.
Blonde Beard's recalled 4,888 bottles of Dojo Asian Wing Sauce sold through multiple retailers in the United States and Canada after confirming undeclared soy on the label. The sauce is shelf-stable and packaged in 8-ounce glass bottles. Consumers should not consume the product and should contact Blonde Beard's for refund or replacement.
Philips North America LLC recalled 1,913,441 IntelliVue Multi Measurement Server X2 M3002A monitors sold to hospitals and healthcare facilities worldwide after reports the devices could fail to alarm. The defect could delay critical warnings for patients. Healthcare facilities should stop using the devices immediately and follow recall instructions from Philips or their healthcare provider.
Philips North America LLC recalled 1,913,441 IntelliVue MP80 patient monitors distributed worldwide to hospitals after reports the devices did not alarm. The defect could prevent alarms from sounding in critical patient situations. Healthcare facilities should stop using the monitors and follow recall instructions from the manufacturer.
Philips North America LLC is recalling 1,913,441 IntelliVue MP5 patient monitors sold to hospitals worldwide. The devices may fail to alarm, delaying detection of patient distress. Hospitals and clinicians should stop using the monitors immediately and follow Philips recall instructions.
Philips North America recalled 1,913,441 IntelliVue MP50 patient monitors worldwide after reports the devices did not alarm. The monitors may fail to alert clinicians to patient deterioration. Hospitals should stop using the devices immediately and follow the manufacturer’s recall instructions.
Philips North America LLC recalled 1,913,441 IntelliVue MP40 patient monitors worldwide after reports the monitors did not alarm. The issue could prevent alerts to clinicians about patient deterioration. Stop using the device and follow the recall instructions from Philips or your healthcare provider immediately.
Milwaukee Tool recalls its M18 FUEL 12" and 14" Top-Handle Chainsaws. The recall covers catalog number 2826-20 with a serial break identified by the 4th digit as 'A'. The chain brake may fail to activate, creating a laceration hazard. Consumers should stop using the recalled chainsaw immediately and contact Milwaukee Tool for a free repair.
HEB recalls a 12-pack Destination Holiday Glow Light Stick Bracelets sold in Texas after the green bracelet can leak and irritate skin. The recall involves bracelets in green, red, pink, orange, yellow and blue colors with UPC 9787014483. Consumers should stop using the green bracelet immediately and return the 12-pack to H-E-B for a full refund.
Olympus Corporation of the Americas recalled 7,803 HX-400U-30 single‑use ligating devices distributed nationwide in the United States. The ligation loop may fail to release or detach. Hospitals and clinics should stop using the device immediately and follow the recall instructions from Olympus or their healthcare providers.
Knog is recalling Blinder 900 and Blinder 1300 Front Bicycle Lights sold at multiple retailers. The recall covers units with batch codes printed on the underside. The lithium-ion battery can overheat and ignite, creating a fire and burn risk. Stop using the recalled lights and register for a free replacement at knog.com/recall.
BBMI Medical recalled 20,694,734 IV administration sets due to backflow risk and occlusion in piggyback configurations. The recall covers sets used with Infusomat Space, Outlook, and Vista Basic Pumps. Stop using the devices immediately and follow manufacturer instructions.
B Braun Medical Inc. recalls 111,312 IV Administration Sets worldwide, including US and international markets, due to backflow risk and occlusion. The recall affects catalog numbers 490193 and 490326, used with Infusomat Space, Outlook, and Vista Basic pumps. Stop using immediately and follow recall instructions for refunds or replacements.
B. Braun Medical recalled 126,050 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The recall cites potential backflow from secondary to primary IV containers and an inability to prime. Health care providers and patients should stop using the device immediately and follow recall instructions from the manufacturer.
B Braun Medical Inc. recalls 168,816 IV administration sets worldwide, including US and international distributors. The recall targets gravity and pump administration sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The issue is potential backflow from piggyback containers into primary IV containers and inability to prime.
B. Braun Medical Inc. recalls 300 extension sets used with Infusomat Space and other pumps. The recall flags potential backflow from piggyback IV containers into primary IV containers and the inability to prime. Hospitals should stop using the device immediately and follow recall instructions.
B Braun Medical Inc recalled 2,544 IV administration sets due to risk of backflow from secondary piggyback containers into primary IV lines and inability to prime. The recall covers products used with BBMI Infusomat Space, Outlook, and Vista Basic pumps and distributed worldwide including the US, Canada, Germany, Guatemala and Singapore. Patients should stop using the device immediately and follow
Mindray DS USA recalled 54 Isoflurane V90 Vaporizers used with the A9 Anesthesia System, distributed worldwide to healthcare providers. The devices have a potential for anesthesia leakage. Clinicians should stop using immediately and contact Mindray DS USA for instructions.
Lannett Company, Inc. recalled 46,848 bottles of NIACIN Extended-release Tablets, 1,000 mg, Rx Only, distributed nationwide. The product failed dissolution specifications. Patients and healthcare providers should stop using it immediately and await recall instructions.
Living Glow recalled for a fire hazard. Guangzhou Jiguang Lighting manufactured the waist fan sold by HSN from May 2025 through July 2025 for $20-$25. Consumers should immediately stop using the recalled device and register for a full refund.
ESR HaloLock wireless power banks were recalled in an expansion that now includes model 2G505. The recall covers models 2G520, 2G505B and 2G512B previously recalled and adds 2G505. The recall is distributed by Waymeet. The lithium-ion batteries can overheat and ignite. Consumers should stop using recalled power banks and seek a full refund from Waymeet.