FDA

FDA (Food and Drug Administration) 注册是指在美国食品药品监督管理局注册或登记某种产品、设备或机构以合法地在美国市场销售、分发或生产。
Ventilator Recall: Smiths Medical Removes ParaPAC Plus Ventilators due to Loosened or Detached Patie

This recall involves removing certain devices from where they are used or sold.

Compounding Device Inlet Correction: Baxter Healthcare Corporation Updates Use Instructions for Exac

This recall involves updating instructions for using devices, and does not invol

Ventilator Correction: Smiths Medical Issues Correction for paraPAC Plus P300 and P310 Ventilators d

Ventilator Correction: Smiths Medical Issues Correction for paraPAC Plus P300 an

Tracheostomy Tube Recall: Smiths Medical Removes BLUselect, BLUgriggs, and BLUperc Tracheostomy Tube

This recall involves removing certain devices from where they are used or sold.

Infusion Pump Battery Recall: ICU Medical Removes Some CSB Batteries Intended For Use With Plum 360,

This recall involves removing certain devices from where they are used or sold.

Early Alert: Endoscope Accessories Forceps/Irrigation Plug Issue from Olympus

This communication is part of the Communications Pilot to Enhance the Medical De

FDA Modernization Efforts for Establishing a Unified Human Foods Program, New Model for Field Operat

The FDA is focused on transforming the agency to be more efficient, nimble and r

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