AEQUITA PHARMACY recalls Tirzepat: 4.4 mg + 1.0mg/0.5 mL injection vials due to lack of processing controls. No remedy stated in official notice.
Lack of Processing Controls.
AEQUITA PHARMACY is recalling a specific injection vial of Tirzepatide and Niacinamide due to a lack of processing controls. This could affect product safety, though the exact risk isn't specified in the recall notice.
The recall states there was a lack of processing controls, which could lead to product contamination or improper manufacturing. However, the exact hazard mechanism isn't detailed in the official notice.
People who have purchased or received this specific injection vial from AEQUITA PHARMACY in the U.S. are affected. Those using the product for medical treatment are most at risk.
Check for the product name: Tirzepatide + Niacinamide 4.4 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial. It was sold by AEQUITA PHARMACY in the U.S. and all lots within expiry.
Identify the specific vial description and manufacturer to confirm if it matches the recalled product.
The official notice does not state any remedy for this recall.
The recall states there was a lack of processing controls, but the exact hazard mechanism isn't detailed in the official notice.
Check for the product name: Tirzepatide + Niacinamide 4.4 mg + 1.0mg/0.5 mL Inj Sol, Inject 0.5 mL (50 units on syringe) subcutaneously, Sterile, 2 mL Multi Dose Vial. It was sold by AEQUITA PHARMACY in the U.S. and all lots within expiry.
We’ve drafted a message you can send AEQUITA PHARMACY to request your refund or repair — edit it as you like.
Subject: Recall D-0555-2025 — AEQUITA PHARMACY AEQUITA PHARMACY Hello, I own a AEQUITA PHARMACY that is covered by recall D-0555-2025 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.
