294 recalls tagged with “battery powered”.
cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
FUNTOK 24V 2-Seater Ride-On Trucks recalled by Shenzhen Luobe Trading Co. for fire and burn hazards. The recall covers model DLS-K03 sold in red, black, white and pink. The company urges consumers to stop using the product and contact for a full refund.
Nexgrill recalls more than 10.2 million metal wire bristle grill brushes sold at Home Depot. Bristles can detach and stick to food or grills. Consumers should stop using recalled brushes and contact Nexgrill for a full refund issued as a gift card.
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Fresenius Kabi USA recalls 0.9% Sodium Chloride Injection units distributed nationwide, including Alaska and Puerto Rico. The recall cites lack of assurance of sterility. Healthcare providers should stop use and contact Fresenius Kabi for guidance.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient statement and allergen information do not include wheat or soy.
This recall involves Cubimana Island Storm 3 In 1 Building Sets. The sets contain 781 pieces of multi-colored building blocks and come in a black box with images of a pirate base and a pirate ship. Model number "HG1004" is printed on the front of the box.
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Lack of Assurance of Sterility
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.