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Connecticut FDA Newswire

  • Published on 14:58 GMT

    FDA Okays DHE Nasal Spray for Acute Migraine

    The US Food and Drug Administration (FDA) has approved dihydroergotamine (DHE) nasal powder (Atzumi, Satsuma Pharmaceuticals Inc) for the acute treatment of migraine with or without aura in adults Atzumi (previously STS101) is the “first and only” product …

    Source: Medscape - Neutral
  • Published on May 4, 2025

    Tomatoes recalled in 14 states due to salmonella risk, FDA says

    Two brands of tomatoes have been recalled in 14 states due to possible salmonella contamination, the Food and Drug Administration said this week. Ray & Mascari Inc. recalled four-count Vine Ripe tomatoes that were sold by Gordon Food Service Stores in …

    Source: CBS News - Neutral
  • Published on May 3, 2025

    Bread Recall After ‘Glass Fragments Found’ Affects 6 States, FDA Says

    There is now a bread recall due to the presence of glass fragments being found on the top of the ... More bread, according to the U.S. Food and Drug Administration. (Photo: Getty)getty You could call this a glass act. There is now a bread recall due to the …

    Source: Forbes - Neutral
  • Published on May 3, 2025

    Do you have this apple juice in your home? FDA says it could make you sick

    More than 170,000 bottles of Martinelli’s apple juice were recently recalled due to concerns of potential contamination with patulin — a type of toxic compound produced by molds and fungi often found in rotten apples and apple products, the Food and Drug …

    Source: SI Live - New York - Neutral
  • Published on May 3, 2025

    FDA Approves Atzumi Nasal Powder for Acute Migraine Treatment

    The US Food and Drug Administration (FDA) has approved Atzumi, a 5.2 mg dihydroergotamine (DHE) nasal powder, for the acute treatment of migraine with or without aura in adults. Developed by Satsuma Pharmaceuticals, Atzumi is the first and only DHE nasal …

    Source: Medical Dialogues - Indeterminate
  • Published on May 2, 2025

    Candy Recall Update as FDA Sets Risk Level

    The Food and Drug Administration (FDA) has classified a Dinstuhl's Fine Candy Company Inc. voluntary recall, that was initiated after undeclared allergens were found in several candy products. The Tennessee-based candy manufacturer started the recall …

    Source: Newsweek - Left-wing
  • Published on May 2, 2025

    FDA resurrects Satsuma's nasal migraine treatment

    More than a year after it was rejected by the FDA, Satsuma Pharma's intranasal migraine therapy Atzumi (formerly STS101) has been given the go-ahead by the agency. The drug – a new dry powder intranasal formulation of the well-established migraine …

    Source: pharmaphorum - Neutral
  • Published on May 2, 2025

    Connecticut neurosurgeon helps stroke patients with rehabilitation device

    A UConn Health neurosurgeon performs procedures that implant a device called a Vivistim, which is a form of Vagus Nerve Stimulation therapy. FARMINGTON, Conn. — A Connecticut neurosurgeon has been a pioneer over the past year in performing procedures that …

    Source: WTIC-TV - Connecticut - Indeterminate
  • Published on May 1, 2025

    FDA Recalls Bread Containing ‘Glass Fragments’

    Over 800 cases of bread are being recalled after “glass fragments” were discovered. The U.S. Food and Drug Administration (FDA) recently categorized the incident as a Class II recall. Here’s how to tell if your bread is included in the recall and what to …

    Source: Prevention - Pending
  • Published on May 1, 2025

    FDA Approves Satsuma’s STS101 Nasal Powder for Acute Migraine

    The FDA has approved Satsuma’s STS101 dihydroergotamine (DHE) nasal powder under the name of Atzumi as a new treatment for adults with acute migraine, with or without aura. The approval is based on positive results from the Phase III ASCEND clinical trial …

    Source: Applied Clinical Trials - Pending
  • Published on May 1, 2025

    FDA Approves Nasal Powder to Treat Migraines

    Satsuma Pharmaceuticals, Inc. announced that the FDA has approved a 505(b)(2) New Drug Application (NDA) for Atzumi™(dihydroergotamine (DHE)) nasal powder for the acute treatment of migraine with or without aura in adults. Atzumi was previously known as …

    Source: American Pharmaceutical Review - Neutral
  • Published on May 1, 2025

    Burger Recall Update as FDA Sets Highest Risk Level

    A recall of seafood burgers has been issued a Class I risk classification by the U.S. Food and Drug Administration (FDA). The recall was initiated earlier this month by the Connecticut based company Caraluzzi's Markets due to the undeclared presence of …

    Source: Newsweek - Left-wing
  • Published on May 1, 2025

    FDA Approves Atzumi, Nasal Powder Formulation of DHE, for Acute Treatment of Migraine

    The FDA approved dihydroergotamine (DHE, formerly STS101; Atzumi; Satsuma Pharmaceuticals), a nasal powder indicated for the acute treatment of migraine with or without aura in adult patients. This approval is supported by findings from a phase 1 …

    Source: Pharmacy Times - Neutral
  • Published on May 1, 2025

    Glass fragments found in bread: FDA recalls products in 6 US states over alarming health risks

    Amid a grave health scare, the US FDA has recalled loaves and rolls sold across six US states, after glass fragments were found in the bread. The federal agency classified the risk as Class I and warned that ingesting glass fragments can “cause injury to …

    Source: The Times of India - Center-right
  • Published on May 1, 2025

    FDA Issues Urgent Recall of Bread That Has Glass Baked Into It!

    The FDA has issued a timely recall on 818 cases of frozen bread due to the potential of glass shards baked into it. "Hey mom, why is my bread crunchy?" You can avoid this question — check the loaves in your home before feeding any bread to your …

    Source: The Wolf - New York - Pending
  • Published on Apr 29, 2025

    Bread sold in six states recalled over ‘glass fragments’: FDA

    An urgent recall has been issued for a bread brand sold throughout the U.S. that could contain “glass fragments,” according to an alert from the US Food and Drug Administration (FDA). The department issued an urgent alert for certain breads that are part …

    Source: New York Post - Right-wing
  • Published on May 4, 2025

    Cleveland’s medical marathon - conquering cancer: Barbara Hertz

    On a spring day in 1941, Cleveland-born Dr. Saul Hertz charged across the Charles River Bridge in Boston with a flask of radioiodine (RAI) he had received from a newly operating cyclotron. There was no time to lose. Elizabeth was waiting, no doubt a little …

    Source: Cleveland.com - Ohio - Neutral
  • Published on Apr 29, 2025

    FDA issues urgent nationwide recall for bread brand sold throughout US

    Check out what's clicking on FoxBusiness.com. An urgent recall has been issued for a bread brand sold throughout the U.S. that could contain "glass fragments," according to an alert from the U.S. Food and Drug Administration (FDA). The …

    Source: FOX Business - Right-wing
  • Published on Apr 28, 2025

    Bread shipments recalled after shards of glass found in packaging: FDA

    A Maryland-based bread company is recalling more than 800 cases of its products, after shards of glass were discovered inside the packaging, according to the Food and Drug Administration. The cases recalled earlier this month by Upper Crust Bakery were …

    Source: SI Live - New York - Neutral

07 days 11:04:08

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