Olympia Pharmacy recalls specific multi-dose vials of papaverine, phentolamine, and atropine due to improper investigation of environmental and personnel monitoring deviations before October 2021. This may affect prescription drug safety.
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 multi-dose vials of papaverine, phentolamine, and atropine that were manufactured before October 2021. The recall is due to quality control issues where monitoring deviations weren't properly investigated, potentially affecting drug safety.
The recall addresses improper investigation of environmental and personnel monitoring deviations before October 2021. This could mean the vials were not properly checked for quality, potentially leading to unsafe drug products.
Prescription drug users who received the specific vials with NDC 73198-0040-10 and lots D41E20, D41F20, G41C13, or G41B13. Patients using these vials for medical treatment are most at risk.
Check for the NDC code 73198-0040-10 and lot numbers D41E20, D41F20, G41C13, or G41B13 on the vial label. These vials were sold by Olympia Pharmacy in Orlando, Florida, with a production date before April 2022.
Look for the NDC code 73198-0040-10 and lot numbers D41E20, D41F20, G41C13, or G41B13 on the vial.
The recall is due to improper investigation of environmental and personnel monitoring deviations before October 2021, which could affect drug safety.
The official notice does not specify a remedy, so contact Olympia Pharmacy directly for guidance.
The recall indicates potential quality control issues, but the official notice does not specify specific safety risks.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0801-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0801-2022 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.
