Family Pharmacy of Statesville recalls Ketamine 50 mg Infusion (LV 1) Solution in 250 mL bags due to lack of sterility assurance. This product is prescription-only and may pose infection risks if used.
Lack of Assurance of Sterility
Family Pharmacy of Statesville is recalling Ketamine 50 mg Infusion (LV 1) Solution in 250 mL bags because they lack sterility assurance. This could lead to infections if the product is used without proper sterilization.
The product lacks assurance of sterility, meaning it may not be free from harmful bacteria or contaminants. If used without proper sterilization, this could lead to infections in patients.
Prescription patients using Ketamine 50 mg Infusion (LV 1) Solution in 250 mL bags from Family Pharmacy of Statesville. Those with the specific lot numbers are most at risk.
Check for the product name: Ketamine 50 mg Infusion (LV 1) Solution in 250 mL bags. Look for lot numbers 07212020@1, 07232020@2, or 07302020@2. The product is prescription-only.
Identify the lot number on the product label to determine if it is recalled.
The recall states there is a lack of assurance of sterility, so it may not be safe to use without proper sterilization.
The recall record does not specify a remedy, so contact Family Pharmacy of Statesville directly for guidance.
Check for lot numbers 07212020@1, 07232020@2, or 07302020@2 on the product label.
We’ve drafted a message you can send Family Pharmacy of Statesville to request your refund or repair — edit it as you like.
Subject: Recall D-0664-2022 — Family Pharmacy of Statesville Family Pharmacy of Statesville Hello, I own a Family Pharmacy of Statesville that is covered by recall D-0664-2022 from Family Pharmacy of Statesville. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.