Olympia Pharmacy recalls zinc chloride vials (NDC 73198-0071-30) due to lack of sterility assurance. This affects prescription-only multi-dose vials sold in Orlando, Florida. Consumers should contact the pharmacy for guidance.
Lack of assurance of sterility.
Olympia Pharmacy is recalling zinc chloride vials that may not be sterile. This poses a risk of infection if used improperly, especially since the vials are multi-dose and intended for prescription use.
The vials lack assurance of sterility, meaning they could contain harmful bacteria. Multi-dose vials increase the risk of contamination when reused multiple times, especially for patients with open wounds or weakened immune systems.
Prescription patients who received the recalled zinc chloride vials from Olympia Pharmacy in Orlando. Those with compromised immune systems or open wounds are at higher risk of infection.
Check for the product name 'Zinc Chloride (0.5 mg/mL), Multi-Dose 30 mL vial, Rx Only' with NDC 73198-0071-30. The vials were sold by Olympia Pharmacy in Orlando, Florida, with lot number K24024 and expiration date 5/24/2022.
Reach out to Olympia Pharmacy at 6700 Conroy Rd., Ste. 155, Orlando, FL 32835 for guidance on next steps.
The recall states there is a lack of assurance of sterility, so the vials may not be safe for use and could cause infection.
Look for the NDC code 73198-0071-30 on the vial label, which was sold by Olympia Pharmacy in Orlando with lot number K24024.
The recall does not specify a discard or return action, so contact Olympia Pharmacy for guidance.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0916-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0916-2022 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.