262 recalls tagged with “lithium battery”.
Reverse Shoulder humeral liners have an articular surface position outside of the dimensional specification within the labeling.
ESR HaloLock wireless power banks, distributed by Waymeet, are recalled. The lithium-ion battery can overheat and ignite, creating a fire and burn hazard. Stop using the recalled power banks and contact Waymeet for a full refund.
undeclared allergen (Wheat and Milk) on ready to eat sandwiches.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Penner Patient Care recalls 190 Bathing Spa devices nationwide after discovering the units lack a unique device identifier. The issue involves missing UDI on the device. Stop using the device immediately and follow the recall instructions.
The device does not bear a unique device identifier.
The device does not bear a unique device identifier.
Product label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: millet and flax
Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate Capsules 40mg, contained Lisdexamphetamine Dimesylate Capsules 30mg.
CGMP deviations: N-nitroso-duloxetine impurity above the proposed interim limit.
CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the established Acceptable Daily Intake (ADI) level.