Jesus fucking Christ. Make Eating Great Again!!!! FDA Response to Imported Foods Potentially Contaminated with Cesium-137 https://www. fda.gov/food/environmental-con taminants-food/fda-response-import
mastodon:mstdn-social 40d ago
A decades-old bug in Knuth's long division (TAOCP Vol II, Algorithm 4.3.1D) L: https:// kolja.rs/algorithm-d/ C: https:// news.ycombinator.com/item?id=4 9286258 posted on 2026.08.13 at 10:11:27 (c=1, p=7)
gov/safety/recal...
The FDA is investigating a new cyclospora outbreak linked to an unknown food source with 72 confirmed illnesses. Unlike previous outbreaks, this one has not been linked to lettuce, leaving health officials searching for the contamination source.
New flu vaccine: Moderna's mRNA vaccine approved by FDA https://www.
Portland man sentenced after strangling female grocery store employee https://www.
The U.S. FDA is investigating a cyclosporiasis outbreak affecting 72 cases across the Midwest with an unidentified source, separate from a prior outbreak. Cases have been reported in Michigan and other states.
The FDA issued a nationwide Class II recall for Levothyroxine sodium tablets manufactured by Major Pharmaceuticals due to subpotency. Patients taking the recalled medication are advised to check their prescription batch numbers and lot codes.
President Trump nominated Dr. Heidi Overton, a White House physician and senior domestic policy aide, to serve as FDA commissioner on August 19, 2026. Overton's nomination drew mixed reception as the administration moved to reshape U.S. health regulations.
US FDA approves Regeneron's rare bone disorder drug Reuters
On 2 September 2026, Marlboro-maker Altria filed suit against the FDA, seeking to force an overhaul of the agency's tobacco product review process, which Altria argues has blocked newer nicotine products from reaching the market.
This cluster aggregates unrelated Oregon news stories: a fatal trench collapse with prior safety warnings in Ohio, a Buc-ee's legal dispute, a Portland city audit finding on contractor waste, Portland Fire basketball players named to FIBA teams, a Portland Trail Blazers player knee injury, and FBI sweeping a university football facility after a coaching departure.
The Rules-Based Nuclear Bomb https://www.
Make Eating Safe Again.
This cluster contains fragmented social media posts from Bluesky and Mastodon with broken links, pixel art shares, and one post referencing fires in Poskot, Odesa during the Ukraine conflict. The posts lack coherent narrative or clear story connection.
Revolution Medicines received FDA approval on August 26, 2026, for daraxonrasib (Rasonque), a once-daily pill that blocks RAS protein variants driving pancreatic cancer growth.
Alibene567:
Cyclospora outbreak followed years of declining FDA foreign inspections AP News
An FDA advisory committee convened for a two-day meeting to consider lifting restrictions on seven peptides that have gained popularity through wellness influencer promotion. The decision could significantly widen public access to these compounds.
FDA approves new imaging agent for Alzheimer's disease detection https://dailyzhealthpress.com/fda-approves-new-imaging-agent-alzheimers/?utm_source=bluesky&utm_medium=social&utm_campaign=zimm-distribute
Former Oregon State QB reportedly named starter at Northwestern https://www.
Federal health officials identified a new outbreak of cyclospora parasite, but the contaminated product source remains unspecified. The FDA is investigating to determine the source of the outbreak.
On 2026-08-24, the U.S. FDA approved the Elecsys pTau217 biomarker blood test developed by Roche and Eli Lilly to identify Alzheimer's-related brain changes in patients aged 55 and older, following European approval in May 2026.
S. regulatory hurdle.
The Food and Drug Administration approved Rasonque (daraxonrasib), a once-daily targeted therapy by Revolution Medicines, on August 26, 2026 for adults with metastatic pancreatic adenocarcinoma. The drug represents the first in its class for this indication.
As of 2026-08-21, President Trump nominated Dr. Heidi Overton, a White House physician serving as deputy assistant to the president for domestic policy, to lead the Food and Drug Administration, which oversees 18,000 staffers regulating food, drugs, and medical devices. Trump pledged to speed approval for new treatments.
Reports on FDA panel approval of unapproved peptide injections favored by RFK Jr. were mixed with an unrelated post about the European Central Bank consulting on new currency designs. These are two separate stories conflated in a single grab-bag cluster.
An FDA advisory committee voted on Thursday to add peptides including BPC-157 and Semax to the list of substances permitted for pharmacy compounding. The vote, which opposed some FDA scientists' positions, would make these peptides more accessible to physicians.
The U.S. Food and Drug Administration approved a new over-the-counter fixed-dose pill combining Tylenol (acetaminophen) with Naproxen, an NSAID. The combination product was approved for nonprescription pain relief.
The FDA issued a nationwide recall of Clear Eyes Maximum Itchy Eye Relief on August 20, 2026, affecting nearly 40,000 bottles due to contamination and sterility concerns. Prestige Brand Holdings voluntarily pulled the batch from store shelves across the United States.