Amneal Pharmaceuticals recalls 1 mL vials of Methylprednisolone Acetate Injectable Suspension due to a typographical error in the NDC number on packaging. Correct NDC is 70121-1574-1; incorrect is 70121-1573-1.
Labeling: Not Elsewhere Classified; A typographical error was observed in the NDC number on the preprinted Individual Folding Cartons (secondary packaging only). Incorrect NDC Number 70121-1573-1; Correct NDC Number 70121-1574-1.
Amneal Pharmaceuticals is recalling certain Methylprednisolone Acetate Injectable Suspension vials because the NDC number on the packaging has a typo. This error could lead to confusion about which vials are legitimate, but it does not pose a safety risk to users.
The recall is due to a typographical error in the NDC number on the secondary packaging. This error could cause confusion about which vials are legitimate, but it does not involve any safety risk to users.
People who own or use the recalled Methylprednisolone Acetate Injectable Suspension vials with the incorrect NDC number 70121-1573-1 are affected. Healthcare providers and patients using the product are most at risk of confusion.
Check the NDC number on the preprinted Individual Folding Carton (secondary packaging). The incorrect NDC number is 70121-1573-1; the correct number is 70121-1574-1. The vials were manufactured with lot numbers AP220481 (expiring 09/2024) or AP220536A (expiring 10/2024).
Look for the NDC number on the preprinted Individual Folding Carton (secondary packaging). The incorrect number is 70121-1573-1; the correct number is 70121-1574-1.
Yes, the product is safe to use. The recall is only due to a typographical error in the NDC number on packaging, which does not affect the product's safety.
Check the NDC number on the secondary packaging. If it's 70121-1573-1, it's recalled; otherwise, it's safe. There is no need to discard the product.
Look for the NDC number on the preprinted Individual Folding Carton (secondary packaging). The recalled vials have the incorrect NDC number 70121-1573-1.
We’ve drafted a message you can send Amneal to request your refund or repair — edit it as you like.
Subject: Recall D-0756-2023 — Amneal Amneal Hello, I own a Amneal that is covered by recall D-0756-2023 from Amneal. 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.
