Kroger Specialty Pharmacy recalls Prolia 60 mg/1 mL PF syringes (NDC 55513-0710-01) due to lack of processing controls. Affected units were dispensed between Dec 2017 and Feb 2018.
Lack of Processing Controls.
Kroger Specialty Pharmacy is recalling Prolia 60 mg/1 mL PF syringes (NDC 55513-0710-01) because of insufficient processing controls. This could lead to medication errors or improper dosing if the syringes are used without proper quality checks.
The recall is due to a lack of processing controls, which could result in medication errors or improper dosing. This means the syringes might not be manufactured to the correct specifications, potentially leading to incorrect medication delivery.
People who received Prolia 60 mg/1 mL PF syringes (NDC 55513-0710-01) from Kroger Specialty Pharmacy between December 2017 and February 2018 are affected. Those using these syringes for hormone therapy are most at risk.
Check for the NDC code 55513-0710-01 on the syringe label. The affected syringes were dispensed by Kroger Specialty Pharmacy between December 2017 and February 2018.
Look for the NDC code 55513-0710-01 on the syringe label to confirm if it's affected.
The recall is due to a lack of processing controls, which could lead to medication errors or improper dosing.
The official notice does not specify a remedy or action for affected syringes.
These syringes were dispensed by Kroger Specialty Pharmacy between December 2017 and February 2018.
We’ve drafted a message you can send Kroger Specialty Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0748-2018 — Kroger Specialty Pharmacy Kroger Specialty Pharmacy Hello, I own a Kroger Specialty Pharmacy that is covered by recall D-0748-2018 from Kroger Specialty 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.
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.