Olympia Pharmacy recalls T-106 vials (NDC 73198-0013-05/10) due to lack of sterility assurance. This medication is for prescription use only and may pose infection risks if used.
Lack of assurance of sterility.
Olympia Pharmacy is recalling T-106 vials containing Papaverine, Phentolamine, and Alprostadil because they lack sterility assurance. This could lead to infections if the medication is used without proper sterility.
The vials lack proper sterility assurance, meaning they could be contaminated with bacteria or other pathogens. This poses a risk of infection if the medication is used without proper sterilization procedures.
Prescription patients who received T-106 vials with NDC numbers 73198-0013-05 or 73198-0013-10 from Olympia Pharmacy in Orlando, FL. Patients using these vials for medical purposes are most at risk.
Check for NDC numbers 73198-0013-05 (5 mL vial) or 73198-0013-10 (10 mL vial) on the packaging. These vials were sold by Olympia Pharmacy in Orlando, Florida, with a lot number of K24F09 and expiration date of November 9, 2022.
Look for NDC numbers 73198-0013-05 or 73198-0013-10 on the vial packaging.
The recall states there is a lack of sterility assurance, which could lead to infection risks. Do not use these vials until the recall is resolved.
Check for NDC numbers 73198-0013-05 (5 mL vial) or 73198-0013-10 (10 mL vial) on the packaging. These vials were sold by Olympia Pharmacy in Orlando, Florida, with a lot number of K24F09 and expiration date of November 9, 2022.
The recall does not specify a remedy, so contact Olympia Pharmacy directly for guidance on safe disposal or alternatives.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0910-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0910-2022 from Olympia 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.
