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FDA, E. coli and McDonald's
E. coli infections tied to McDonald's burgers rise to 75, US FDA says
Oct 25 (Reuters) - The number of people infected by the E. coli outbreak tied to McDonald's (MCD.N) Quarter Pounder hamburgers increased to 75 from 49, the U.S. Food and Drug Administration said on Friday.
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.
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 recalls over 7,000 bottles of antidepressant
FDA recalls duloxetine, antidepressant known as Cymbalta, over possible cancerous chemical
The U.S. Food and Drug Administration has recalled over 7,000 bottles of the antidepressant duloxetine, which is commonly sold under the name Cymbalta. According to the FDA, the drug was recalled because it had the "presence" of N-nitroso-duloxetine, a nitrosamine, which is a chemical that could increase the risk of cancer.
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.
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 certain types of bacterial urinary tract infections (UTI) in adult women, the health regulator said on Friday.
Iterum Therapeutics Gets FDA Approval Of Orlynvah For Treatment Of Urinary Tract Infections
This is the first approved indication for Orlynvah and the first FDA-approved product for Iterum. "We are so pleased to have achieved this historic milestone and would like to thank all the patients,
1d
FDA probing McDonald's supplier Taylor Farms as source of E. Coli outbreak, CNBC reports
The U.S. Food and Drug Administration was investigating whether Taylor Farms, a supplier for McDonald's , was the possible ...
Managed Healthcare Executive
1h
FDA Approves IV Form of Stelara Biosimilar Selardsi
This week’s approval expands Seldardsi indications to treat adults with Crohn’s disease and ulcerative colitis.
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 ...
dvm360
8h
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 ...
TCTMD
7h
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
8h
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 ...
8h
MrBeast's Lunchly Meal Brand Reportedly Hit By FDA Complaints, Claims of Mold
The brand was launched last month by Logan Paul, KSI, and MrBeast.
FierceBiotech
11h
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.
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