Pharmacy Innovations recalls 10mg/0.25mg/ml injectable chlorpheniramine/hyoscyamine due to FDA finding of insanitary conditions at manufacturing facility. This product is for prescription use only.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling a prescription injectable medication because FDA inspections found unsanitary conditions at their Erie, PA facility. This could lead to contamination of the product, posing a risk of infection or illness if used.
FDA inspections found unsanitary conditions at the manufacturing facility, which could lead to contamination of the product. This contamination risk means the medication might not be sterile when administered, potentially causing infections or other health issues.
Prescription patients who received this specific injectable medication from Pharmacy Innovations in Erie, PA. Those with medical conditions requiring this medication are at higher risk.
This product is labeled as Chlorpheniramine/Hyoscyamine (1ML) 10MG/0.25MG/ML Injectable, Rx Only. It was manufactured by Pharmacy Innovations at 2936 W 17th St., Erie, PA.
Look for the product name and address on the label to confirm it matches the recalled item.
FDA inspections found unsanitary conditions at the manufacturing facility, which could lead to contamination of the product.
The recall notice does not specify a remedy.
This product is labeled as Chlorpheniramine/Hyoscyamine (1ML) 10MG/0.25MG/ML Injectable, Rx Only, manufactured by Pharmacy Innovations at 2936 W 17th St., Erie, PA.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0186-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0186-2023 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.
