DNR: Zebra mussel larvae reported in Phalen chain of lakes in Ramsey County

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Zebra mussel larvae has been found in Lake Gervais and Spoon Lake, according to the Minnesota Department of Natural Resources. The lakes are part of the Phalen chain of Lakes in Ramsey County, between Little Canada and Maplewood.

State officials had taken water samples from Lake Gervais, Kohlman Lake, Keller Lake and Spoon Lake to check for zebra mussel larvae. While larvae were found in Lake Gervais and Spoon Lake, adult zebra mussels have not been detected. Nevertheless, the larvae indicates zebra mussel presence. The two lakes — as well as the connecting lakes Kohlman and Keller — will be listed as infested.

To prevent the spread of invasive species, the DNR asks people to:

• Clean watercraft, trailers and equipment to remove aquatic plants and prohibited invasive species.

• Drain all water and leave drain plugs out when moving watercraft and get rid of unwanted bait in the trash.

• Never release bait, plants or aquarium pets into state waters.

• Use dry docks, lifts and rafts for 21 days before moving watercraft from one waterbody to another. Also, spray down watercraft and equipment with high-pressure hoses or rinse them off with water.

There are free stations to decontaminate watercraft around the state — for more information go to the DNR website.

Anyone thinking they have found zebra mussels or other invasive species can contact the DNR at dnr.state.mn.us/invasives/ais/contacts.html.

More information can be found at mndnr.gov/ais.

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Longtime St. Paul coffee shop Kopplin’s to close next month

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After nearly 20 years in St. Paul, Kopplin’s coffee shop will pour its last cup next month.

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While owners Andrew and Amanda Kopplin plan to continue roasting coffee and selling beans online and via wholesale, they’re shutting down the Marshall Avenue cafe and walk-up window when their lease ends, they announced on social media. An exact closing date has not been announced but is expected to be in October.

“For many reasons, (this) is the best move for us at this time,” the pair wrote online. “Wherever you stopped along your journey, thanks for sharing a cup with us! We hope you’ll stop by the window if you’re around, and we’ll see your names on our shipping and subscription lists into the future.”

The Kopplins did not respond to a request for comment.

Andrew Kopplin opened his namesake coffee shop in April 2006 in Highland Park and moved to the current Marshall Avenue spot in 2011. During those early years, Kopplin’s was one of the first and only places in the Twin Cities to find specialty or “third-wave” coffee roasted in small batches.

That style of coffee is popular now but, outside of a few places like Spyhouse and Peace Coffee in Minneapolis and JS Bean Factory and to some extent Dunn Brothers in St. Paul, was not well-known or understood in the early 2000s. So there was just as much education going on in the snug Highland Park shop as coffee-brewing, Andrew Kopplin told the Pioneer Press in 2007.

“If you can get people through it and they like what you’re doing, they’re a very devoted customer because there’s no one else that does it. But you have to get them here,” he said at the time.

Kopplin’s: 2038 Marshall Ave.; 651-808-0958; kopplinscoffee.com

FDA takes aim at Hims and other telehealth services in drug advertising blitz

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By MATTHEW PERRONE, AP Health Writer

WASHINGTON (AP) — For the first time, federal health officials are taking aim at telehealth companies promoting unofficial versions of prescription drugs — including popular weight loss medications — as part of the Trump administration’s crackdown on pharmaceutical advertising.

The Food and Drug Administration on Tuesday posted more than 100 letters to various drug and online prescribing companies, including Hims & Hers, which has built a multibillion-dollar business centered around lower-cost versions of blockbuster obesity injections.

The FDA warned the company to remove “false and misleading” promotional statements from its website, including language claiming that its customized products contain “the same active ingredient” as FDA-approved drugs Wegovy and Ozempic. The formulations cited by regulators are produced by specialty compounding pharmacies and aren’t reviewed by the FDA.

“Your claims imply that your products are the same as an FDA-approved product when they are not,” states the warning letter, dated Sept. 9.

San Francisco-based Hims said Tuesday that it “looks forward to engaging with the FDA.”

“Our website and our customer-facing materials note that compounded treatments are not approved or evaluated by the FDA,” the company said in a statement.

It’s the first FDA attempt to directly police online platforms like Hims, which have long argued they’re not subject to traditional drug advertising rules.

A memo signed by President Donald Trump last week directed Health Secretary Robert F. Kennedy Jr. and the FDA to ensure that pharmaceutical ads on TV, social media and other websites are “truthful and non-misleading.” As part of the initiative, the FDA promised to send 100 letters to companies with deceptive ads.

The new FDA letters each contain “cease and desist” language. That’s a different approach for the agency, which typically drafts its letters in highly bureaucratic language citing specific FDA regulations.

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Hims has been under scrutiny from Washington for months.

Earlier this year, a Super Bowl ad from the company touted the benefits of its weight-loss medications but didn’t list any of their side effects or potential harms. FDA rules require advertisements to present a balanced picture of drug risks and benefits.

Makary singled out the ad in last week’s Journal of the American Medical Association, calling it a “brazen” example of how advertising is “contributing to America’s culture of overreliance on pharmaceuticals for health.”

Hims and similar companies initially sold cheap generic versions of drugs for hair loss, erectile dysfunction and other health issues. But booming demand for obesity medications opened the door to selling cheaper copies.

The FDA permits so-called compounding, or customized production, when there is a shortage of the official versions of FDA-approved medications.

FDA recently determined that the GLP-1 drugs no longer met the criteria for a shortage. That should have ended the compounding, but there is an exception: The practice is still permitted when a prescription is customized for the patient.

Hims and other companies have taken to offering “personalized” dosages and formulations for certain patients, arguing they offer extra benefits.

The letters posted Tuesday come from FDA’s drug center.

A letter posted last week from FDA’s vaccine division took issue with a TV ad for AstraZeneca’s FluMist vaccine, saying the spot’s “background music and visual distractions” detract from information about side effects. The letter was signed by FDA vaccine chief Dr. Vinay Prasad, an ally of Kennedy who recently returned to his job at the agency after briefly being forced to step aside.

Researchers and consumer advocates have long complained that the upbeat TV images of patients enjoying life with family and friends often overshadow discussions of side effects.

Additionally, studies have shown that patients exposed to drug ads are more likely to ask their doctors about the medication, even if they don’t fit the prescribing criteria. The American Medical Association, the nation’s largest physician group, came out in support of a ban in 2015, citing TV advertising’s role in “inflating demand for new and more expensive drugs.”

The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Science and Educational Media Group and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.

Fed convenes meeting with a governor newly appointed by Trump and another he wants to oust

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By CHRISTOPHER RUGABER, AP Economics Writer

WASHINGTON (AP) — After a late-night vote and last-minute ruling, the Federal Reserve began a key meeting on interest rate policy Tuesday with both a new Trump administration appointee and an official the White House has targeted for removal.

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Stephen Miran, a top White House economist who was confirmed by the Senate with unusual speed late Monday, was sworn in Tuesday as a member of the Fed’s board of governors. He will vote on the Fed’s interest rate decision on Wednesday, when the central bank is expected to reduce its key rate by a quarter-point. Miran may dissent in favor of a larger cut.

Also attending the meeting is Fed governor Lisa Cook, whom the Trump administration has sought to fire in an unprecedented attempt to reshape the Fed, which historically is considered independent of day-to-day politics. An appeals court late Monday upheld an earlier ruling that the firing violated Cook’s due process rights. A lower court had earlier also ruled that President Donald Trump did not provide sufficient “cause” to remove Cook.

Stephen Miran testifies during a Senate Banking Committee hearing on his nomination to be a member of the Board of Governors of the Federal Reserve System, on Capitol Hill Thursday, Sept. 4, 2025, in Washington. (AP Photo/Mariam Zuhaib)

With both officials in place, the Fed’s two-day meeting could be unusually contentious for an institution that typically prefers to operate by consensus. It’s possible that as many as three of the seven governors could dissent from a decision to reduce rates by just a quarter-point in favor of a half-point. That would be the first time since 1988 that three governors have dissented. Economists also say that one of the five regional Fed bank presidents who also vote on rates could dissent in favor of keeping rates unchanged.

On Tuesday, the White House said it would appeal Cook’s case to the Supreme Court, though did not specify when.

“The President lawfully removed Lisa Cook for cause,” White House spokesman Kush Desai said. “The Administration will appeal this decision and looks forward to ultimate victory on the issue.”