Pharmacy Innovations recalls SCOPOLAMINE HYDROBROMIDE 0.25% OPH SOLUTION (Rx Only) due to FDA finding insanitary conditions at the manufacturing facility. Consumers should check product details and contact the company for guidance.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling SCOPOLAMINE HYDROBROMIDE 0.25% OPH SOLUTION (Rx Only) because FDA inspections found unsanitary conditions at the facility. This could lead to contamination risks for users.
FDA inspections found unsanitary conditions at the manufacturing facility, which could lead to contamination of the product. This poses a risk of infection or other health issues if the medication is used without proper sterility.
People who have the SCOPOLAMINE HYDROBROMIDE 0.25% OPH SOLUTION (Rx Only) prescription medication from Pharmacy Innovations. Those with medical conditions requiring this medication are at higher risk.
Check for the product name 'SCOPOLAMINE HYDROBROMIDE 0.25% OPH SOLUTION' with 'Rx Only' label. The medication was sold by Pharmacy Innovations at their Erie, PA facility.
Look for the product name 'SCOPOLAMINE HYDROBROMIDE 0.25% OPH SOLUTION' with 'Rx Only' label.
FDA inspections found unsanitary conditions at the manufacturing facility, which could lead to contamination risks.
The recall record does not specify a remedy.
Check for the product name 'SCOPOLAMINE HYDROBROMIDE 0.25% OPH SOLUTION' with 'Rx Only' label from Pharmacy Innovations.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0235-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0235-2023 from Pharmacy Innovations. 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.
