Teva recalls 15mg amphetamine tablets with incorrect strength label
Teva Pharmaceuticals recalls 100-count amphetamine tablets labeled 15mg but containing 20mg tablets. This label error may lead to incorrect dosing. Consumers should check their bottles for the specific lot number.
Lower-risk recall
Labeling: Label Error on Declared Strength; A sealed 100-count bottle labeled with 15 mg actually contained 100 tablets of 20 mg strength of the drug product.
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What happened, in plain English
Teva Pharmaceuticals is recalling 100-count amphetamine tablets that were labeled as 15mg but actually contain 20mg tablets per bottle. This label error could lead to incorrect dosing if taken without knowing the actual strength. Read more at govinfonow.com/recall/34336-teva-recalls-15mg-amphetamine-tablets-with-incorrect-strength-label.
Source Summary by GovInfoNow · govinfonow.com/recall/34336-teva-recalls-15mg-amphetamine-tablets-with-incorrect-strength-label · Updated August 18, 2026 · FDA enforcement record: FDA #D-1539-2022
Cite this page
“Teva recalls 15mg amphetamine tablets with incorrect strength label.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/34336-teva-recalls-15mg-amphetamine-tablets-with-incorrect-strength-label. Based on FDA recall #D-1539-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1539-2022%22&limit=1).
Why it’s dangerous
The tablets are labeled as 15mg but contain 20mg strength. This label error means users might take a higher dose than intended, which could lead to incorrect dosing if not noticed.
Who’s affected
People who own or use these specific amphetamine tablets for medical purposes. Those with a prescription for this medication are most at risk due to potential dosing errors.
How to tell if you have this one
Check for the specific lot number 100023340 on the bottle. The product is a 100-count bottle labeled 15mg but contains 20mg tablets. It was sold by Teva Pharmaceuticals in North Wales, PA.
- Brand
Teva- Category
Drug
What to do — step by step
Check Product Label
Look for the lot number 100023340 on the bottle to confirm if it's part of the recall.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide in the US.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 11 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1539-2022 (August 29, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1539-2022 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.