95,089 total recalls in our database
Stryker Medical Division of Stryker
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Vyaire Medical
Two patient circuits, 29028-003 and 29028-004, for the 3100 High Frequency Oscillatory ventilator that are only approved for use outside the U.S. were distributed in the U.S.
Stryker Medical Division of Stryker
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Stryker Medical Division of Stryker
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Remington Medical
There is an error with the "Use by Date" and "Date of Manufacturer" on the box label.
Potentially defective utility trays in the reagent kits.
Wilson-Cook Medical
Nonconforming devices while manufactured correctly, do not comply to their design requirements. Potential harms associated with balloon detachment are endoscopic retrieval of an impacted or non-impacted object, bleeding caused by the retrieval device, or the incident can occur without injury and the object is left to pass naturally.
Pump not detected as connected to controller due to software issue.
Ortho Clinical Diagnostics (QuidelOrtho) confirmed during routine testing that some lots from Coating 3598 of VITROS ECO2 slides included carts which may contain consecutive slides that may not function as intended. These affected slides (potentially intermittent, consecutive slides within a cart or across consecutive carts) have an abnormality which may cause positively or negatively biased total carbon dioxide (CO2) results leading to either overdiagnosis of acidosis or missing alkalosis, both which may prompt unnecessary therapies such as IV fluids and/or bicarbonate or overdiagnosis of alkalosis which may also result in unnecessary use of IV fluids and electrolyte replacement or failure to detect acidosis and necessary treatment.
Integra LifeSciences
Defect in the outer packaging of the Cranial Access Kits. can cause the packaging to split without any additional forces outside compromising the sterility of the device
Stryker Medical Division of Stryker
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Staar Surgical Company
Their is a potential that intraocular implant devices may not meet specifications.
Unknown Manufacturer
In "parent-facing" mode, the backrest of the seat can move downward, placing the infant in a negative recline. In this situation, an unrestrained infant could tumble from the seat, posing an injury hazard.
SLIS, of China
The bulbs can overheat when the string lights are plugged directly into an outlet, presenting burn and fire hazards.
Unknown Manufacturer
The wire tool attachment can break when dropped while tethered to a tool exceeding two pounds, posing an injury hazard to bystanders.
Unknown Manufacturer
The eyes of the plush toys can break off, posing a choking hazard to young children.
Unknown Manufacturer
The recalled mattresses violate multiple provisions of the federal safety regulation for crib mattresses, including the thickness test and missing warnings and labels. The product poses a suffocation hazard to infants.
Unknown Manufacturer
The mattresses fail to meet the mandatory federal flammability standard for mattresses, posing a fire hazard.
Unknown Manufacturer
The vacuum's electric cord plug prong can detach and remain in an electrical outlet when the vacuum is unplugged. This poses an electrical shock hazard to consumers.
Unknown Manufacturer
The bottom portion of the recalled baby rattles can detach, posing choking and/or ingestion hazards.