Revive Rx recalls specific Tirzepatide 10mg/0.5mL vials due to potential sub-potent drug levels. Affected units were compounded by Revive Rx Pharmacy in Houston, TX. Consumers should contact the manufacturer for details.
Sub-potent Drug
Revive Rx is recalling Tirzepatide 10 mg/0.5 mL vials that may contain less active drug than intended. This could lead to ineffective treatment for diabetes or obesity. The recall is for compounded products sold with specific lot and expiration dates.
The vial may contain less active drug than labeled, which could result in the medication not working as intended. This might lead to inadequate treatment for conditions like diabetes or obesity. However, the risk is not severe enough to cause serious injury.
People who have received the specific Tirzepatide vial from Revive Rx Pharmacy in Houston, TX. Those with diabetes or obesity who use this medication are most at risk.
Check for the vial labeled 'Tirzepatide 10 mg/0.5 mL Sterile Solution-2 mL Vial, Rx Only, For Sub-Q Use Only' compounded by Revive Rx Pharmacy. The lot number 1643397 and expiration date 10/16/2023 are specific identifiers.
Look for the lot number 1643397 and expiration date 10/16/2023 on the vial label.
The recall states there is a risk of sub-potent drug levels, but the product is not unsafe to use. The manufacturer recommends checking the specific lot and expiration details.
Check for the vial labeled 'Tirzepatide 10 mg/0.5 mL Sterile Solution-2 mL Vial, Rx Only, For Sub-Q Use Only' with lot number 1643397 and expiration date 10/16/2023.
The recall does not specify a remedy, so contact Revive Rx Pharmacy directly for further instructions.
We’ve drafted a message you can send Revive Rx to request your refund or repair — edit it as you like.
Subject: Recall D-0771-2023 — Revive Rx Revive Rx Hello, I own a Revive Rx that is covered by recall D-0771-2023 from Revive Rx. 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.
