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U.S. Food and Drug Administration

Stories that name U.S. Food and Drug Administration.

Checked 7 min ago · 32 of 35 sources responding · Sources and method

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U.S. Food and Drug Administration

Recall U.S. Food and Drug Administration (Recalls)

Global Mix Inc. Recalls Niwali Tejocote Capsules and Niwali Tejocote Pieces Because of Possible Health Risk

Global Mix Inc. of Middle Village, New York, is recalling niwali Tejocote Capsules (90 capsules, Herbal Supplement) and niwali Tejocote Pieces (90 Day Supply, Herbal Supplement) because FDA analysis has determined that the products appear to be Thevetia peruviana, or yellow oleander. All parts of th

AgencyU.S. Food and Drug AdministrationRecalls and safety alerts

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Recall U.S. Food and Drug Administration (Recalls)

A&P Creations LLC Issues Nationwide Recall of biQ-FEL Due to Undeclared Sildenafil and Tadalafil

Sildenafil and Tadalafil are active ingredients in FDA-approved prescription drugs Viagra and Cialis, respectively, used to treat erectile dysfunction. FDA approval of Viagra and Cialis is restricted to use under the supervision of a licensed health care professional. These undeclared ingredients ma

AgencyU.S. Food and Drug AdministrationRecalls and safety alerts

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Recall U.S. Food and Drug Administration (Recalls)

Wakefern Food Corp. Voluntarily Recalls Wholesome Pantry Organic Unsweetened Apple Sauce

KEASBEY, N.J. (Sept. 14, 2026) –Wakefern Food Corp. has voluntarily recalled select containers of Wholesome Pantry Organic Unsweetened Apple Sauce after routine FDA testing identified elevated patulin levels that exceed food safety limits and do not meet Wakefern's quality standards

AgencyU.S. Food and Drug AdministrationRecalls and safety alerts

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Recall U.S. Food and Drug Administration (MedWatch)

BMC Medical Co., Ltd. Recalls Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect

On July 15, 2026, BMC Medical Co., Ltd. (BMC), Beijing, China, retrospectively reported to the US Food and Drug Administration (FDA) a recall of 20,160 Luna G3 APAP (Model LG3600) devices distributed in the United States due to firmware defect. This corrective action was not reported to customers. O

AgencyU.S. Food and Drug AdministrationRecalls and safety alerts

Read at U.S. Food and Drug Administration (MedWatch)