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FDA, E. coli and McDonald
As FDA probes source of national E. coli outbreak, California firm recalls onion products
Salinas-based international food production giant Taylor Farms had announced a recall on four onion products 'due to potential E. coli contamination.'
FDA investigates onion supplier in McDonald's E. coli outbreak
The FDA says it is focusing on a California company that sells McDonald's and other restaurants onions. McDonald's says California-based Taylor Farms is the source of the potentially tainted onions on its Quarter Pounders in some states.
McDonald’s outbreak news: What to know about E. coli cases, onions, recalls, more
Seventy-five people across 13 states have fallen ill in an E. coli outbreak attributed to McDonald's Quarter Pounders.
Iterum Therapeutics Gets FDA Approval Of Orlynvah
FDA Approves Novel Treatment for UTIs
The FDA approved oral sulopenem etzadroxil and probenecid (Orlynvah) to treat uncomplicated urinary tract infections (uUTIs) caused by certain bacteria in women with limited or no alternative oral antibacterial treatment options, the agency said Friday.
US FDA approves Iterum's treatment for urinary infection
The U.S. Food and Drug Administration has approved Iterum Therapeutics' oral antibiotic to treat a type of urinary tract infection (UTI) in adult women, the health regulator said on Friday. The drug has been approved to treat uncomplicated UTIs,
Iterum Therapeutics announces FDA approval of Orlynvah
Iterum Therapeutics (ITRM) plc announced that the U.S. Food and Drug Administration has approved Iterum’s new drug application for
FDA recalls thousands of antidepressant bottles
FDA Duloxetine recall flags 7,100+ bottles of generic Cymbalta antidepressants
A Duloxetine recall by the FDA has flagged more than 7,100 bottles of the Cymbalta generic drug due to a cancerous chemical.
FDA Has Recalled Thousands of Bottles of Antidepressant Duloxetine, Sold Under Brand Name Cymbalta: Here’s Why
The Duloxetine Delayed-Release Capsules' voluntary recall began on Oct. 10 after the FDA deemed the medication the second-highest risk classification. Over 7,100 bottles of Duloxetine were recalled, including 500 delayed-release 20mg capsules. The lot number is 220128, and the expiration date is 12/2024, per the FDA report.
FDA recalls over 7,000 bottles of antidepressant due to possible cancerous chemical
The FDA has recalled thousands of bottles of the antidepressant duloxetine, sold under brand name Cymbalta, due to the presence of a possibly cancer-causing chemical.
dvm360
5h
FDA: Off-label use of aspirin in lactating dairy cattle is prohibited
Vazalore is currently the only FDA-approved human aspirin that may be used in food-producing animals under certain conditions ...
Yahoo
5h
MrBeast's Lunchly Meal Brand Reportedly Hit By FDA Complaints, Claims of Mold
The complaints come on the heels of reports of moldy snack kits that have turned up on social media over the past week. The ...
Cure Today
1d
FDA Accepts New Drug Application for Pixclara for Glioma Imaging
Pixclara, a glioma-imaging agent, has been granted priority review by the
FDA
with a decision deadline of April 26, 2025.
FierceBiotech
8h
FDA approves Medtronic's Affera all-in-one pulsed field ablation system
Less than a year after obtaining an FDA approval for its first foray into pulsed field ablation, Medtronic has done it again.
STAT
15h
Eli Lilly weight loss drug shortage underscores deeper issues with FDA oversight
A turbulent series of events around the supply of Eli Lilly’s blockbuster weight loss treatment has raised concerns around ...
TCTMD
4h
Michelle Tarver Named New FDA Director of Medical Devices
Tarver, an ophthalmologist, replaces longtime CDRH Director Jeff Shuren, who announced his retirement in July.
JD Supra
5h
FDA Finalizes Guidance on Use of Part 11 Electronic Systems, Records and Signatures in Clinical Investigations
On October 1, 2024, the US Food and Drug Administration (FDA) finalized its guidance on the use of electronic records in clinical investigations ...
MedPage Today
1d
FDA Warns Companies Over Products Made With Amniotic Fluid
These warning letters are the latest in a series of FDA efforts to crack down on companies selling birth-tissue-derived ...
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