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。
Baxter Issues Urgent Device Correction to Reinforce Important Safety Information Regarding Cleaning

SummaryCompany Announcement Date:October 28, 2020FDA Publish Date:October 29, 20

BD Announces Voluntary Recall on Intraosseous Products

SummaryCompany Announcement Date:June 22, 2022FDA Publish Date:June 22, 2022Prod

Abbott Recalls the Readers used with the FreeStyle Libre, FreeStyle Libre 14 day, and FreeStyle Libr

On April 12, 2023, the FDA added information for patients about Abbott’s April 2

Nurse Assist, LLC Issues Recall of 0.9% Sodium Chloride Irrigation USP and Sterile Water for Irrigat

SummaryCompany Announcement Date:November 06, 2023FDA Publish Date:November 06,

Recall of Certain Saline and Sterile Water Medical Products Associated with Nurse Assist: FDA Safety

Update: April 15, 2024Additional Related Recalls of Saline and Sterile Water Med

Do Not Use Cardinal Health Monoject Syringes with Syringe Pumps and PCA Pumps - Letter to Health Car

UPDATE: February 2, 2024On February 2, 2024, Cardinal Health announced a recall

Cardinal Health Recalls Sterile Monoject Luer-Lock and Enteral Syringes Due to a Change in Manufactu

UPDATE: March 7, 2024Cardinal Health is expanding their previous product correct

Olympus Corporation of the Americas Recalls Bronchofiberscopes and Bronchovideoscopes Because They C

The FDA has identified this as a Class I recall, the most serious type of recall

Cardinal Health Issues Medical Device Recall for Nurse Assist Products Contained Within Kits/Trays

SummaryCompany Announcement Date:December 21, 2023FDA Publish Date:February 05,

Smiths Medical ASD Inc. Recalls Medfusion Model 4000 Syringe Pump Due to Issues Associated with Earl

Please be aware, this recall is a correction, not a product removal.The FDA has

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