Olympia Pharmacy recalls specific multi-dose vials of At-1 medication due to improper investigation of environmental and personnel monitoring deviations before October 2021. This affects certain lots with specific NDC numbers.
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 a multi-dose vial of At-1 medication (Papaverine, Phentolamine, Atropine) because quality control issues occurred before October 2021. This recall is for patients who have this specific medication prescribed by a doctor.
The recall is due to quality control issues where environmental and personnel monitoring deviations were not properly investigated before October 2021. This could potentially lead to medication safety problems if the vials were used without proper quality checks.
Patients with a prescription for this specific multi-dose vial from Olympia Pharmacy are affected. Those who have the vial with NDC 73198-0039-10 and lots F41C28 or F41B28 are most at risk.
Check your prescription label for the product name 'At-1', which includes Papaverine 8mg/ml, Phentolamine 2mg/ml, and Atropine 0.2mg/ml. Look for the NDC number 73198-0039-10 and lots F41C28 or F41B28.
Verify if your prescription contains the specific multi-dose vial with NDC 73198-0039-10 and lots F41C28 or F41B28.
The recall indicates potential quality control issues, but the official notice does not specify if the medication is safe to use without the recall.
Check your prescription label for the product name 'At-1' with specific NDC number 73198-0039-10 and lots F41C28 or F41B28.
The official recall notice does not specify a remedy, so you should 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-0802-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0802-2022 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.
