95,018 total recalls in our database
Not programmed in accordance with specification. The programming affects the RFID function and does not allow the NanoKnife probes to be recognized by the NanoKnife generator resulting in a delay in procedure
Encore Medical
Patella drills are marked with incorrect diameter size of 5.6mm, when they should be 5.4mm. Porous patella overdrills are marked with incorrect diameter size of 5.4 mm, when they should be 5.6 mm. If the incorrect drill is selected during surgery, there is risk of the implant loosening, implant not properly fitting, and/or fractured bone.
Coloplast Manufacturing US
A decrease in wall thickness has the potential for a premature pump failure, compared to a pump with standard wall thickness, based on the number of interactions with the pump to inflate and deflate the penile prosthesis.
A service unit was potentially improperly tested and calibrated during manufacturing on a failed test station.
Coloplast Manufacturing US
A decrease in wall thickness has the potential for a premature pump failure, compared to a pump with standard wall thickness, based on the number of interactions with the pump to inflate and deflate the penile prosthesis.
Unknown Manufacturer
The recalled children's bathrobes fail to meet the federal flammability standards for children's sleepwear, posing a risk of burn injuries to children.
Unknown Manufacturer
The children's nightgowns fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries to children.
Unknown Manufacturer
The recalled children's robes fail to meet the federal flammability standards for children's sleepwear, posing a risk of burn injuries to children.
Luxor Workspaces LLC, of Waukegan, Illinois
The recalled audiovisual (A/V) carts can become unstable when loaded with heavy objects, such as cathode-ray tube televisions (CRT TVs). When loaded with heavy objects such as CRT TVs, the recalled A/V carts pose a tip-over hazard to children, which can result in serious injury or death.
Moen Incorporated, of North Olmsted, Ohio
The lithium-ion battery back-up can overheat, posing a fire hazard.
Infant Formula has the potential to be contaminated with Cronobacter spp.
Wismettac Asian Foods
Product was found to have the incorrect crustacean named on products
The firm was notified by a customer that the outer case label indicates the product contains eggs. However, the primary product label does not include egg in the ingredient list.
Desserts by Helen
Product contained JIF peanut butter and was manufactured during the JIF recall time period in 2022. Product was recalled out of an abundance of caution.
Wismettac Asian Foods
Product was found to have the incorrect crustacean named on products
Cashews declared in ingredients statement but not in the contains statement.
DFA Dairy Brands Fluid
1% Low Fat Milk potentially contaminated with sanitizer
Possible contamination with Listeria monocytogenes
CGMP Deviations: Repackaging firm recalling due to potential product cross contamination concerns at the manufacturer.
Preferred Pharmaceuticals
cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection.