Labor leader David Huerta was detained while observing Immigration and Customs Enforcement raids taking place in Los Angeles.

The Service Employees International Union California (SEIU) says that its president was injured during the ICE raids and is calling for his release, NBC4 Los Angeles reports.

“SEIU California members call for the immediate release of our President, David Huerta, who was injured and detained at the site of one of today’s ICE raids in Los Angeles. He is now receiving medical attention while in custody,” Tia Orr, Executive Director of SEIU California, said.

Mayor Karen Bass told NBC4 that Huerta had been pepper-sprayed during the incident.

“He is doing ok physically, but I know what really impacted him the most was the emotional trauma of watching parents and kids being separated,” Bass said. “He’s going into ICE custody and we hope to get him out very soon.”

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The mayor said she does not know why Huerta is being detained.

The SEIU issued a statement supporting Huerta, insisting that he was “exercising his First Amendment right to observe and document law enforcement activity.”

“We are proud of President Huerta’s righteous participation as a community observer, in keeping with his long history of advocating for immigrant workers and with the highest values of our movement: standing up to injustice, regardless of personal risk or the power of those perpetrating it,” the union said.

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Orr also condemned the ICE raids.

“We call for an end to the cruel, destructive, and indiscriminate ICE raids that are tearing apart our communities, disrupting our economy, and hurting all working people. Immigrant workers are essential to our society: feeding our nation, caring for our elders, cleaning our workplaces, and building our homes,” she said.

Bass said she is going to meet with immigrant support groups to discuss plans for responding to situations like the mass ICE raids in the future.

“My message to them is that we are going to fight for all Angelenos regardless of when they got here, whether they have papers or not,” she said. “We are a city of immigrants, and this impacts hundreds of thousands of Angelenos.”

ICE arrested approximately 44 people in Friday’s raid, according to Homeland Security Investigations.

“Today, ICE officers and agents alongside partner law enforcement agencies, executed four ​federal search warrants at three location in central Los Angeles. Approximately 44 people were administratively arrested ​​and one arrest for obstruction. The investigation remains ongoing, updates will follow as appropriate,” HSI spokesperson Yasmeen Pitts O’Keefe said in a statement.

COMPTON, Calif. (KABC) — Governor Gavin Newsom toured Clinton Elementary School in Compton Thursday, recognizing Compton Unified School District’s recent gains in academic scores, while also pushing his statewide education goals.

“We have seen academic growth that outpaces almost all districts in the state of California and across the nation,” said Dr. Darin Brawley, the Compton Unified School District Superintendent.

Brawley hosted Newsom, who was pushing his Golden State Literacy Plan, a promise to continue increasing California’s rising reading skills.

The price tag is well into the billions of dollars, a bold move during a time when California is facing a $12 billion drop in state revenues.

Among the programs Newsom is funding, there is one that would reduce the student-teacher ratio from 12-to-1 to 10-to-1. Another program funds Transitional Kindergarten classes in every school district. And at the cost of $4.4 billion, Newsom wants “After School for All” and “Summer School for All” programs to begin.

“Nine hours a day of enriched learning opportunity and a minimum of 30 days during the summer of subsidized learning,” Newsom touted. “Unprecedented in California history.”

Newsom mentioned that his own struggles with dyslexia have spurred his determination to increase literacy in California.

“People were persistent and had my back, and people didn’t give up on me,” Newsom said about how he was able to overcome the learning disability. “I struggle with it every single day. There’s not a day where my dyslexia does not expose itself.”

California and three other states petitioned the U.S. Food and Drug Administration Thursday to ease its new restrictions on the abortion pill mifepristone, citing the drug’s proven safety record and arguing the new limits are unnecessary.

“The medication is a lifeline for millions of women who need access to time-sensitive, critical healthcare — especially low-income women and those who live in rural and underserved areas,” said California Atty. Gen. Rob Bonta, who filed the petition alongside the attorneys general of Massachusetts, New York and New Jersey.

The petition cites Senate testimony by Health and Human Services Secretary Robert F. Kennedy Jr. last month, in which Kennedy said he had ordered FDA administrator Martin Makary to conduct a “complete review” of mifepristone and its labeling requirements.

The drug, which can be received by mail, has been on the U.S. market for 25 years and taken safely by millions of Americans, according to experts. It is the most common method of terminating a pregnancy in the U.S., with its use surging after the Supreme Court overturned Roe vs. Wade in 2022.

The Supreme Court upheld access to the drug for early pregnancies under previous FDA regulations last year, but it has remained a target of anti-abortion conservatives. The Trump administration has given Kennedy broad rein to shake up American medicine under his “Make America Healthy Again” banner, and Kennedy has swiftly rankled medical experts by using dubious science — and even fake citations — to question vaccine regimens and research and other longstanding public health measures.

At the Senate hearing, Kennedy cited “new data” from a flawed report pushed by anti-abortion groups — and not published in any peer-reviewed journal — to question the safety of mifepristone, calling the report “alarming.”

“Clearly, it indicates that, at very least, the label should be changed,” Kennedy said.

Sen. Josh Hawley (R-Mo.) on Monday posted a letter from Makary to X, in which Makary wrote that he was “committed to conducting a review of mifepristone” alongside “the professional career scientists” at the FDA.

Makary said he could not provide additional information given ongoing litigation around the drug.

The states, in their 54-page petition, wrote that “no new scientific data has emerged since the FDA’s last regulatory actions that would alter the conclusion that mifepristone remains exceptionally safe and effective,” and that studies “that have frequently been cited to undermine mifepristone’s extensive safety record have been widely criticized, retracted, or both.”

Democrats have derided Kennedy’s efforts to reclassify mifepristone as politically motivated and baseless.

“This is yet another attack on women’s reproductive freedom and scientifically-reviewed health care,” Gov. Gavin Newsom said the day after Kennedy’s Senate testimony. “California will continue to protect every person’s right to make their own medical decisions and help ensure that Mifepristone is available to those who need it.”

Bonta said Thursday that mifepristone’s placement under the FDA’s Risk Evaluation and Mitigation Strategy program for drugs with known, serious side effects — or REMS — was “medically unjustified,” unduly burdened patient access and placed “undue strain on the nation’s entire health system.”

He said mifepristone “allows people to get reproductive care as early as possible when it is safest, least expensive, and least invasive,” is “so safe that it presents lower risks of serious complications than taking Tylenol,” and that its long safety record “is backed by science and cannot be erased at the whim of the Trump Administration.”

The FDA has previously said that fewer than 0.5% of women who take the drug experience “serious adverse reactions,” and deaths are exceedingly rare.

The REMS program requires prescribers to add their names to national and local abortion provider lists, which can be a deterrent for doctors given safety threats, and pharmacies to comply with complex tracking, shipping and reporting requirements, which can be a deterrent to carrying the drug, Bonta said.

It also requires patients to sign forms in which they attest to wanting to “end [their] pregnancy,” which Bonta said can be a deterrent for women using the drug after a miscarriage — one of its common uses — or for those in states pursuing criminal penalties for women seeking certain abortion care.

Under federal law, REMS requirements must address a specific risk posed by a drug and cannot be “unduly burdensome” on patients, and the new application to mifepristone “fails to meet that standard,” Bonta said.

The states’ petition is not a lawsuit, but a regulatory request for the FDA to reverse course, the states said.

If the FDA will not do so nationwide, the four petitioning states asked that it “exercise its discretion to not enforce the requirements” in their states, which Bonta’s office said already have “robust state laws that ensure safe prescribing, rigorous informed consent, and professional accountability.”