Teva Pharmaceuticals recalls 1.62% testosterone gel with OOS viscosity. This may affect product stability. Consumers should check NDC 0591-2926-30 and lot number 100029472.
OOS for viscosity
Teva Pharmaceuticals is recalling testosterone gel due to viscosity issues that could affect product stability. This recall affects prescription-only products sold in specific packaging.
The gel has an out-of-specification viscosity, which may cause the product to separate or become unstable over time. This could affect the medication's effectiveness but does not pose an immediate safety risk.
Prescription users of Teva's testosterone gel (1.62% CIII) with NDC 0591-2926-30 and lot number 100029472. Patients using this product are most at risk.
Check for the NDC code 0591-2926-30 and lot number 100029472 on the packaging. This product is sold in 30-unit-dose packets per carton, prescription-only.
Look for NDC 0591-2926-30 and lot number 100029472 on the packaging.
The recall is for viscosity issues that may affect product stability, but the product is not unsafe for use. Consumers should check the NDC and lot number.
The recall does not specify a remedy, so no action is required beyond checking the product details.
Check for NDC 0591-2926-30 and lot number 100029472 on the packaging. This product is sold in 30-unit-dose packets per carton, prescription-only.
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-0127-2024 — Teva Teva Hello, I own a Teva that is covered by recall D-0127-2024 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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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.
