Testosterone Cypionate, 200 mg/mL, packaged in a) 5 mL… was recalled on October 9, 2026 in cooperation with the U.S. Food and Drug Administration because lack of sterility assurance..
Testosterone Cypionate, 200 mg/mL, packaged in a) 5 mL vials (NDC 73271-1225-1) and b) 30 m vials ( NDC 73271-1226-2) This Is A Compounded Dug, Intramuscular Use, Office Use Only, 8400 Esters Blvd, STE 190, Irving, TX 75063.
a) Lot 10212025@3, BUD 10/21/2026; 10292025@4, BUD 10/29/2026; 10282025@6, BUD: 10/29/2026; 12012025@1, BUD: 12/01/2026; 04072026@1, BUD: 04/01/2027; 05262026@3, BUD 05/08/2027; 05262026@7, BUD 11/17/2026; 05272026@1, BUD 05/08/2027; 05272026@2, BUD: 11/22/2026; 07032026@1, BUD 05/08/2027; 07022026@1, BUD: 05/08/2027; 07062026@3, BUD: 05/08/2027; 07072026@3, BUD: 12/30/2026. b) 04012026@2, BUD 04/01/2027.
Units affected: 4675 vials
Where it was sold: Nationwide in the USA.
Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.
Lack of sterility assurance.
Class II means the product might cause a temporary or medically reversible health problem; the chance of serious harm is remote.
Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.
Contact: Recalling firm: Right Value Drug Stores LLC
Not sure what you're entitled to? Read our guide: what to do if your product is recalled.
Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.
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