95,018 total recalls in our database
Edwards Lifesciences
There is a potential that the pressure tubing may detach from the blood sampling system
Due to external labelling error/mix-up. Affected product external labels list the incorrect rod size.
Significant wear of the Monitor Bracket Assembly shaft goes unrecognized could potentially lead to the Monitor Bracket Assembly detaching from the Suspension Arm and result in potential hazard for the monitor to fall while remaining attached to the cables resulting in patient, operator, bystander, or service person to serious injury.
Philips North America
Significant wear of the Monitor Bracket Assembly shaft goes unrecognized could potentially lead to the Monitor Bracket Assembly detaching from the Suspension Arm and result in potential hazard for the monitor to fall while remaining attached to the cables resulting in patient, operator, bystander, or service person to serious injury.
Edwards Lifesciences
There is a potential that the pressure tubing may detach from the blood sampling system
The supplier informed them of possible deviations of the parameters/processes defined for ethylene oxide sterilization.
The HAT trial contains a retaining ring that has shown the potential to disengage during use.
Edwards Lifesciences
There is a potential that the pressure tubing may detach from the blood sampling system
Philips North America
Significant wear of the Monitor Bracket Assembly shaft goes unrecognized could potentially lead to the Monitor Bracket Assembly detaching from the Suspension Arm and result in potential hazard for the monitor to fall while remaining attached to the cables resulting in patient, operator, bystander, or service person to serious injury.
Bard Access Systems
Catheter kits contained the incorrect micro-introducers.
Edwards Lifesciences
There is a potential that the pressure tubing may detach from the blood sampling system
A portion of a validation lot was inadvertently released to the US Market. The product did not meet the validation testing criteria regarding leakage.
One lot number of a specific model of ULTRAperc Percutaneous Dilation Tracheostomy Kit, 9.0mm may have been incorrectly labeled as a 7.0mm ID kit.
Physician Order Form (PL-15400-00 Nov 2018) distributed is discontinued due to the text 'Refill the pump and program refill with the same medication removed prior to MRI' may be misinterpreted as 'reuse the same drug solution extracted from the pump prior to the MRI procedure', creating a possible risk of infection
Shanghai Unitex Apparel, of Shanghai, China
The children's robes fail to meet the federal flammability standards for children's sleepwear, posing a risk of burn injuries to children.
Unknown Manufacturer
The glue on the back of the mirrors can fail causing the mirror to detach and fall out of the frame, posing laceration and injury hazards.
TBD Liquids LLC, of Santa Rosa, Calif.
Liquid nicotine must be in special packaging as required by the Child Nicotine Poisoning Prevention Act (CNPPA). The packaging of the products is not child-resistant, posing a risk of poisoning if the contents are swallowed or touched by young children. Liquid nicotine is toxic if ingested or absorbed through the skin or eyes.
Banner Smoked Fish
Product may be contaminated with Listeria monocytogenes.
Products are deficient in multiple nutrients required for infant formula, and the firms contract manufacturer does not test for Cronobacter, a pathogen that can be particularly dangerous to infants and is sometimes found in powdered infant formulas.
Possible metal fragments in Yogurt Bars