COVID-19 Update
Mon, 07 Dec 2020 00:00:00 -0500
Italiano
Mon, 07 Dec 2020 00:00:00 -0500
The FDA is informing of a potential for injury during MRI while wearing a face mask that contains metal (such as surgical or non-surgical masks and respirators).
The FDA is updating our October 28, 2019 safety communication on the use of AFX endovascular grafts with Duraply material (AFX with Duraply or AFX2).
WishGarden Herbs, Inc. is voluntarily recalling, to the consumer level, 14 lots of Cord Care and Goldenseal Powder products produced after 7/26/18 with expiration dates between 7/26/18 and 9/1/20.
Mesquite, TX MPM Medical is voluntarily recalling one lot of Regenecare HA Hydrogel to the consumer level. Following two customer complaints of visible contamination, the product was found to be contaminated with the bacteria Burkholderia cepecia.
Baxter Sigma Spectrum Infusion Pumps w/ Master Drug Library (V. 6 & 8) and Spectrum IQ Infusion Systems with DoseIQ Safety Software deliver fluids into the body
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