Recall Ledger

Isotretinoin Capsules recall (Teva Pharmaceuticals USA, Inc)

DrugClass IIOngoing

Summary: Teva Pharmaceuticals USA, Inc is recalling Isotretinoin Capsules, USP, 30 mg, Rx Only, 10 count Prescription Pack, Manufactured for: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 0591-2435-15 (carton), NDC 0591-2435-45 (blister pack).. Reason: Superpotent and Subpotent.

What is being recalled

Isotretinoin Capsules, USP, 30 mg, Rx Only, 10 count Prescription Pack, Manufactured for: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 0591-2435-15 (carton), NDC 0591-2435-45 (blister pack).

Why

Superpotent and Subpotent

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

FL, OH, PR & MS (states named: Florida, Mississippi, Ohio, Puerto Rico)

How to tell if yours is affected

Lots 100055426, Exp. date 02/2026, 100071518, Exp. date 04/2027 & 100072450, Exp. Date 07/2027

What to do

Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.

Recall facts

Recall numberD-0445-2026
CategoryDrug
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedJanuary 12, 2026
ReportedApril 15, 2026
CompanyTeva Pharmaceuticals USA, Inc
Company locationParsippany, NJ, United States
Initiated byVoluntary: Firm initiated
Quantity21984 packages

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Official FDA record