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The insulin syringes should not be used because the skewed markings could lead to the patient getting the wrong dose of insulin, resulting in serious harm or death. Read More
The mandatory reporting requirements “have been essential during the COVID-19 pandemic,” the agency said, noting that the information received from hospitals enabled the agency to assess risks more quickly. Read More
Medtronic has ceased distribution and marketing of the system and has issued a letter requesting that physicians stop implants of the device. Read More
Patients should keep consumer electronics six inches away from their implanted devices and avoid carrying electronics in a pocket over the implant, the agency said. Read More
China’s National Medical Products Administration reported that in 2020, the country’s medical device adverse event monitoring system received a total of 536,055 medical device adverse event reports, an increase of more than 35 percent on the previous year. Read More
China’s National Medical Products Administration reported that in 2020, the country’s medical device adverse event monitoring system received a total of 536,055 medical device adverse event reports, an increase of more than 35 percent on the previous year. Read More
The FDA’s Medical Devices Advisory Committee recommended in a March 23 meeting that patients have their vision evaluated before periocular treatment with dermal fillers. Read More
The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) said that paclitaxel drug-coated balloons or drug-eluting stents should not be used in the routine treatment of patients with widening of the arteries, as the mortality risk generally outweighs the benefits. Read More