Family Pharmacy of Statesville recalls Hydromorphone HCl 0.1 mg/mL Infusion in 1000 mL bags due to lack of sterility assurance. This product is for prescription use only and was manufactured with specific lot and expiration dates.
Lack of Assurance of Sterility
Family Pharmacy of Statesville is recalling Hydromorphone HCl 0.1 mg/mL Infusion in 1000 mL bags because they lack sterility assurance. This means the product could cause infections if used improperly. The recall is for prescription-only use.
The product lacks sterility assurance, meaning it could be contaminated with bacteria or other pathogens. This contamination could lead to infections if the medication is administered to patients. The hazard is specific to the infusion product and not applicable to other medications.
Prescription patients using Hydromorphone HCl 0.1 mg/mL Infusion in 1000 mL bags from Family Pharmacy of Statesville are affected. Healthcare providers who dispensed this product may also be at risk.
Check for the product name: Hydromorphone HCl 0.1 mg/mL Infusion in 1000 mL bags. The lot number is 08022020@1 and the expiration date is 8/17/2020. This product is for prescription use only.
Look for the lot number 08022020@1 and expiration date 8/17/2020 on the product label.
The recall states there is a lack of sterility assurance, which means the product could be contaminated and cause infections. It is not safe to use without contacting the manufacturer.
The recall does not specify a remedy, so contact Family Pharmacy of Statesville directly for guidance.
The recall mentions a lack of sterility assurance, which could lead to infections, but the record does not specify the risk of serious injury.
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-0659-2022 — Family Pharmacy of Statesville Family Pharmacy of Statesville Hello, I own a Family Pharmacy of Statesville that is covered by recall D-0659-2022 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.
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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.
