Olympia Pharmacy recalls Formula F9 vials (NDC 73198-0004-10) produced before October 2021 due to improper investigation of environmental and personnel monitoring deviations. No immediate health risk reported.
CGMP Deviations: prior to October 1, 2021, environmental and personnel monitoring Out of Action Limit (OOAL) excursions were not being properly investigated
Olympia Pharmacy is recalling Formula F9 vials that were manufactured before October 2021 because their quality control process failed to properly investigate monitoring deviations. This could potentially lead to unsafe drug concentrations, but no injuries have been reported.
The vials were manufactured before October 2021 when the pharmacy's quality control process failed to properly investigate environmental and personnel monitoring deviations. This could result in improper drug concentrations, but no injuries have been reported.
Prescription patients who received Formula F9 vials with NDC 73198-0004-10 produced before October 2021. Healthcare providers using these vials for medical treatments are most at risk.
Check for vials labeled 'Formula F9, Papaverine 0.9mg/ml . Phentolamine 0.1mg/ml . PGE 20mcg/mL Atropine 0.01mg/ml, Multi-Dose 10 ml vial, Rx' with NDC 73198-0004-10. Look for batch numbers D41C19, I42C13, or I42B13.
Identify the NDC code (73198-0004-10) and batch numbers (D41C19, I42C13, I42B13) on the vial label.
The recall is due to manufacturing monitoring issues, but no injuries have been reported. The product may still be safe if used properly.
Check for NDC 73198-0004-10 with batch numbers D41C19, I42C13, or I42B13.
The recall does not specify a return or disposal action, so contact Olympia Pharmacy directly 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-0800-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0800-2022 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.
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.
