95,018 total recalls in our database
Boston Scientific
Stryker Neurovascular has observed that certain lots of Guider Softip XF Guide Catheters appear to have the incorrect tip curve shape. The impacted products were distributed with a tip curve shape which differs from the labeled tip curve shape.
Ortho Clinical Diagnostics (QuidelOrtho) confirmed certain Proboscis/Piston Assemblies manufactured between 07-Apr-2022 (Date code: 040722) and 19-Dec-2022 (Date code: 121922) may not perform as intended due to an out-of-specification barrel component. This may cause VITROS VersaTips and/or VITROS MicroTips to be improperly seated on the proboscis, which may result in falsely elevated Gentamicin and Valproic Acid assay results as well as an increased frequency of condition codes resulting in delayed patient results. The issue was identified by internal testing when reported instruments failed to pass release testing and were traced to the molded Proboscis part J56639 with date codes from 040722 onward.
Skin grafts thin and non-uniform when using the affected blades. The issue would be identified at the time of use and may result in the need for additional harvests to adequately cover the area
In rare occasions, the combination of a leak of a highly flammable solvent at the ion source probe, and an electrical discharge may result in a flame on top of the probe and possible ejection of the electrode assembly from the probe. There is a risk to the patient/user, customer property, or environment because there is a potential for a health risk and property damage should the flame be left unattended. The failure causes a delay in patient results.
Boston Scientific
Stryker Neurovascular has observed that certain lots of Guider Softip XF Guide Catheters appear to have the incorrect tip curve shape. The impacted products were distributed with a tip curve shape which differs from the labeled tip curve shape.
Under certain conditions, an issue might prevent the device from performing as intended. A specific sequence of commands on the control unit activates the traction drive and triggers an unintended driving (autodrive) of max. 7 sec. may result in the following reasonably foreseeable injury or damage to the health of patients and/or users
ARROW INTERNATIONAL
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Unknown Manufacturer
The candy's rolling ball can detach from the product's container into a child's mouth, posing a choking hazard for consumers.
Unknown Manufacturer
The recalled children's blanket sleepers and robes fail to meet the federal flammability standards for children's sleepwear, posing a risk of burn injuries to children.
Unknown Manufacturer
The candy's rolling ball can dislodge from the product into a child's mouth, posing a choking hazard or death.
Unknown Manufacturer
The recalled pet products can contain bacteria, including Pseudomonas aeruginosa, an environmental organism found widely in soil and water. People with weakened immune systems or external medical devices who are exposed to Pseudomonas aeruginosa face a risk of serious infection that may require medical treatment. The bacteria can enter the body if inhaled, through the eyes, or through a break in the skin. People with healthy immune systems are usually not affected by the bacteria.
Unknown Manufacturer
The internal circuit board components can overheat, posing a fire hazard.
Vitality Works
Foreign material: pieces of a pen (writing utensil).
Vitality Works
Foreign material: pieces of a pen (writing utensil).
ICE CREAM HOUSE
Products may be contaminated with Listeria monocytogenes.
Vitality Works
Foreign material: pieces of a pen (writing utensil).
Vitality Works
Foreign material: pieces of a pen (writing utensil).
Vitality Works
Foreign material: pieces of a pen (writing utensil).
Vitality Works
Foreign material: pieces of a pen (writing utensil).
Products may be contaminated with Listeria monocytogenes.