1,215 recalls tagged with “replacement available”.
Philips recalled 1,913,441 IntelliVue MX600 patient monitors distributed worldwide after reports that the devices did not alarm. The defect could prevent alarms that alert clinicians to patient distress. Hospitals and clinicians should stop using the devices immediately and follow the recall instructions from Philips North America LLC.
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 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 is recalling 1,913,441 IntelliVue MP2 patient monitors worldwide. The devices may fail to alarm when critical conditions arise. Hospitals should stop using the monitors and follow Philips recall instructions.
Aizu Olympus recalled 6,578 OER-Elite medical devices distributed nationwide in the United States. The recall cites warnings, cautions, and maintenance requirements and says only trained personnel should perform repairs. Healthcare providers and patients should stop using the device and await recall instructions from the manufacturer.
Philips recalls 1.913 million IntelliVue MP20 patient monitors worldwide because the devices may fail to alarm. The issue could prevent critical alerts from sounding. Hospitals should stop using the monitors immediately and follow Philips recall instructions.
Philips North America is recalling 1,913,441 IntelliVue MP60 patient monitors. The monitors may fail to alarm as designed. Hospitals and clinics using MP60 units should stop using the devices and follow the 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.
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 MX100 patient monitors due to potential alarm failure. The recall is active as of December 2025. The manufacturer warns patients and healthcare providers to stop using affected devices and follow recall instructions. Contact Philips North America LLC for guidance.
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.
STRYKER recalled 39,148 NICO Myriad Handpieces sold worldwide due to latex in packaging that could trigger allergic reactions. The latex-containing tape secures components within packaging. Healthcare providers and patients should stop using the device immediately and follow the recall instructions from Stryker.
Werner Paddles recalls Stealth and Covert kayak paddles after determining they can break during use, creating a drowning hazard. The paddles sold by retailers nationwide and online from October 2023 through August 2025 for $470 to $560. Consumers should stop using the recalled paddles immediately and contact Werner Paddles for a full refund or store credit.
Crate & Barrel recalled Ana Dining Chairs sold at Crate & Barrel stores and Crateandbarrel.com from January 2021 through January 23, 2025 for a fall hazard. The chair legs can break, posing a fall risk. Stop using the recalled chair and contact Crate & Barrel to obtain a free replacement chair and arrange a free pickup.
Grundens has issued an active recall for the Youth Clipper 282 Jacket and the Youth Zenith 282 Jacket in youth sizes 8 through 12. The jackets have hood drawstrings that can catch on objects, creating a risk of strangulation. Consumers should stop using the jackets immediately and contact Grundens for a full refund or a 20% store credit after removing the drawstrings.
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.
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.
Harppa recalled 5-in-1 convertible high chairs due to risk of serious injury or death from fall and entrapment hazards. The recall involves model BHC001 with production batch 202408. The chairs were sold in green, pink and gray. Consumers should stop using the product immediately and seek a replacement. Harppa provides a replacement option and destruction instructions for the recalled unit.
B Braun Medical recalls 19,104 IV Administration Sets distributed worldwide, including the United States and international distribution to Canada, Germany, Guatemala, and Singapore. The recall cites backflow of medication from secondary piggyback IV containers into primary IV lines and an inability to prime due to occlusion. The affected catalog number is 490400. Stop using the device and follow a