Teva Pharmaceuticals USA Inc recalls Tretinoin Capsules, 10 mg, Rx Only, 100 capsules per bottle, Teva Pharmaceuticals USA Inc., North Wales, PA, 19454, NDC
Teva recalls 10mg Tretinoin Capsules due to failed dissolution testing. This affects specific lots from 2022-2023. Consumers should contact Teva for details.
Lower-risk recall
Failed Dissolution Specifications; Low Out of Specification (OOS) results for dissolution.
Contact the company & request your remedy
What happened, in plain English
Teva is recalling 10mg Tretinoin Capsules that failed dissolution testing. This means the medication may not work as intended for patients using it as prescribed. Read more at govinfonow.com/recall/34620-teva-tretinoin-capsules-10mg-recall-failed-dissolution-testing.
Source Summary by GovInfoNow · govinfonow.com/recall/34620-teva-tretinoin-capsules-10mg-recall-failed-dissolution-testing · Updated September 23, 2026 · FDA enforcement record: FDA #D-1156-2022
Cite this page
“Teva Tretinoin Capsules 10mg Recall: Failed Dissolution Testing.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/34620-teva-tretinoin-capsules-10mg-recall-failed-dissolution-testing. Based on FDA recall #D-1156-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1156-2022%22&limit=1).
Why it’s dangerous
The capsules failed dissolution testing, meaning they may not release the medication properly in the body. This could lead to inconsistent dosing but does not cause immediate harm.
Who’s affected
Prescription patients using Teva's 10mg Tretinoin Capsules. Those with specific lot numbers from 2022-2023 are most at risk.
How to tell if you have this one
Check the bottle for the lot numbers: 100022971 (expires 08/2022), 100022972 (expires 05/2023), or 100028920 (expires 09/2023).
- Brand
Teva- Category
Drug
What to do — step by step
Check Product Lot Number
Look for the lot numbers on the bottle: 100022971, 100022972, or 100028920.
Questions people ask
What is the recall for?
Teva is recalling 10mg Tretinoin Capsules that failed dissolution testing, affecting specific lot numbers from 2022-2023.
How do I know if I have the recalled product?
Check the bottle for lot numbers: 100022971 (expires 08/2022), 100022972 (expires 05/2023), or 100028920 (expires 09/2023).
What should I do if I have the recalled product?
The recall record does not specify a remedy, so contact Teva directly for instructions.
Contact Teva
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-1156-2022 — Teva Teva Hello, I own a Teva that is covered by recall D-1156-2022 from Teva. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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-1156-2022 (June 14, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1156-2022 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 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.