AEQUITA PHARMACY recalls Tirzepat: 8.8 mg + 1.0mg/0.5 ml injection vials due to lack of processing controls. No remedy specified in official notice.
Lack of Processing Controls.
AEQUITA PHARMACY is recalling Tirzepatide and Niacinamide injections because of processing control issues. This could affect product safety, though no specific harm is mentioned in the recall.
The recall states 'Lack of Processing Controls' but does not explain how this could cause harm. Without details on the hazard mechanism, the risk level cannot be determined.
People who own or use this medication from AEQUITA PHARMACY. Those with the specific injection vial size and lot numbers are most at risk.
Check for the AEQUITA PHARMACY brand, 8.8 mg Tirzepatide + 1.0mg Niacinamide injection vials, and the specific lot numbers listed in the recall notice.
Identify the brand, product name, and lot number to confirm if your item is affected.
The official notice does not specify any remedy.
The recall states 'Lack of Processing Controls' but does not explain how this could cause harm.
Check for the AEQUITA PHARMACY brand, 8.8 mg Tirzepatide + 1.0mg Niacinamide injection vials, and the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send AEQUITA PHARMACY to request your refund or repair — edit it as you like.
Subject: Recall D-0557-2025 — AEQUITA PHARMACY AEQUITA PHARMACY Hello, I own a AEQUITA PHARMACY that is covered by recall D-0557-2025 from AEQUITA PHARMACY. 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.
