95,102 total recalls in our database
O&M HALYARD
Surgical drape packs may have open seals, which may compromise the sterility of the product.
Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
Potential that a component (air baffle) may be missing in some Nehalem FlexVision-2 PCs that are part of the Allura Xper series.
Boston Scientific has identified a higher likelihood of air embolism events when procedures are performed without positive pressure-controlled ventilation. According to published literature and clinical data, in percutaneous procedures requiring transseptal access to the left atrium when conscious or deep sedation is used, patients have an approximately three-times higher risk (U.S. study) of negative left atrium pressure and air ingress. This risk is especially prevalent in patients with pre-existing low left atrial pressure, hypovolemia, and partial upper airway collapse.
Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.
Medtronic Perfusion Systems
The catheters may not retain their shape.
DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
Unknown Manufacturer
The flexible grease gun hose can develop a hole allowing grease to be ejected while using the grease gun, posing a laceration hazard.
StopBox USA, of Spokane Valley, Washington
A manufacturing defect allows the recalled chamber locks to be forcibly removed, allowing unauthorized or unintended access to the firearm, posing a risk of serious injury or death.
Unknown Manufacturer
The baby loungers violate the mandatory standard for Infant Sleep Products because the sides are shorter than the minimum side height limit to secure the infant; the sleeping pad's thickness exceeds the maximum limit, posing a suffocation hazard; and an infant could fall out of an enclosed opening at the foot of the lounger or become entrapped. The portable loungers do not have a stand, posing a fall hazard. These violations create an unsafe sleeping environment for infants, posing a risk of serious injury or death.
CHETAK NEW YORK
Product tested positive Salmonella .
Gelson branded Hummus product labels do not include storage instructions "keep refrigerated"
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Bakers Authority
Product label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: millet and flax
Mold. The firm noticed an increase in customer complaints. They conducted a root cause investigation and discovered that one of their coolers had malfunctioning.
Product may be contaminated with Cesium-137 (Cs-137)
DFA Dairy Brands
Product contains undeclared wheat and soy.
Bakers Authority
Product label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: poppy seeds, dried garlic, dried onion, and sea salt
Middlefield Original Cheese Cooperative
Potential contamination with Listeria monocytogenes