FDA Recalls Popular ADHD Medications
Growing Up, I Had No Clue What ADHD Even Was
When I was growing up, ADHD was not something anyone talked about. Looking back, there were definitely a few kids who probably had it and would have benefited from medication, but none of us knew what we were seeing. My husband was one of those kids. He struggled all through school and finally got diagnosed as an adult. He still takes medication today.
Just last night, we sat down to do a simple task on the computer, and I had to remind him over and over to come sit down and finish it with me. He was too busy checking noises, looking for raccoons out the window, doing literally anything except staying focused. His medication had worn off, and the ADHD was shining bright!
Why I Have Zero Problem Talking About It
Before anyone comes at me for talking about his diagnoses, just know he is the first person to tell anyone he has ADHD, and that medication makes a huge difference for him. Our daughter has the exact same diagnosis and treatment plan. When either of them forgets their meds, friends, teachers, co-workers and I can instantly spot it, and we have reminded them more than once to go take their pill. Hey, it takes a village, y'all!
Because my daughter is still in school, I am the one who manages most of her care. I work closely with her doctor to keep her on the smallest dose that still helps her. She tells me when she is having trouble focusing at certain times of day, and we make adjustments together. It is very much a team effort. The point is, a person who has been diagnosed with ADHD (and sometimes the people around them) can pretty quickly tell when their medication dosage is off. We are also very vocal about the fact that it's nothing to be ashamed of. Their brains work differently, and they need meds to quiet all the noise.
FDA Issues Recall On Popular ADHD Medication
Unfortunately, the FDA announced that anyone taking lisdexamfetamine dimesylate (the generic version of Vyvanse) needs to double-check their bottles. Some capsules were not dissolving the right way, which means the medication may not work like it is supposed to.
Sun Pharmaceutical Industries in New Jersey issued a voluntary recall for certain bottles of the medication. The recall started October 28 and the FDA labeled it a Class II risk on October 30.
The affected lot numbers and expiration dates are:
10mg: AD42468 (exp. 2/28/2026), AD48705 (exp. 4/30/2026);
20mg: AD42469 (exp. 2/28/2026), AD48707 (exp. 4/30/2026);
30mg: AD42470 (exp. 2/28/2026), AD48708 (exp. 4/30/2026);
40mg: AD48709 (exp. 4/30/2026), AD50894 (exp. 5/31/2026);
50mg: AD48710 (exp. 4/30/2026), AD50895 (exp. 5/31/2026);
60mg: AD48711 (exp. 4/30/2026), AD50896 (exp. 5/31/2026); and
70mg: AD48712 (exp. 4/30/2026), AD50898 (exp. 5/31/2026).
What This Means For People Who Take It
Since the medication may not dissolve correctly, people could notice that it feels weaker or less effective. The good news is that there is no dangerous risk, but it can absolutely affect focus, mood, and daily functioning.
There was no public press release from Sun Pharmaceuticals, so the advice has been to contact your doctor and pharmacy directly. They can help with how to proceed with dosage, refunds, replacements, and how to safely dispose of the recalled medication.
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