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November 17, 2023 at 9:58 AM. (Reuters) - The U.S. Food and Drug Administration (FDA) on Friday said it had identified the recall of B. Braun Medical Inc's medicine-delivering pump system as most ...
The U.S. Food and Drug Administration issued a Class I recall, the agency's most serious, for the Medfusion syringe pump, the third major FDA recall for the line of devices made in Oakdale. Smiths ...
Many Medicare beneficiaries and their caregivers don’t, however, so they never receive emails or letters about the potential hazards. ECRI called gaps with recalls of home-use medical devices ...
Recall information. FDA develops a strategy for each individual recall that sets forth how extensively it will check on a company's performance in recalling the product in question. For a Class I recall, for example, FDA would check to make sure that each defective product has been recalled or reconditioned. In contrast, for a Class III recall ...
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]
Adult trauma level. Pediatric trauma level. University of Alabama at Birmingham Hospital. Birmingham. Alabama. 1295. I. Huntsville Hospital & HH for Women & Children. Huntsville.
The recall by the U.S. Food and Drug Administration of one medical company's entire line of infusion pumps -- widely used to administer fluids to the human body -- has called attention to ...
Ifosfamide (IFO), sold under the brand name Ifex among others, is a chemotherapy medication used to treat a number of types of cancer. [2] This includes testicular cancer, soft tissue sarcoma, osteosarcoma, bladder cancer, small cell lung cancer, cervical cancer, and ovarian cancer. [2] It is administered by injection into a vein.