Pharmacy Innovations recalls Bupren: 0.9mg/ml injectable vials due to FDA finding insanitary conditions. Risk of contamination during manufacturing.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling Buprenorphine HCL 0.9 MG/ML (25ML vial) injectables because FDA found insanitary conditions at their facility. This could lead to contamination risks for patients using the medication.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility. This means the injectable vials could be contaminated during production, posing a risk of infection or other health issues for patients.
Patients prescribed this medication by a healthcare provider. Those using the product without medical supervision are not affected.
Check for the Buprenorphine HCL 0.9 MG/ML (25ML vial) Injectable, Rx Only label. The product was manufactured by Pharmacy Innovations at 2936 W 17th St., Erie, PA.
Look for the Buprenorphine HCL 0.9 MG/ML (25ML vial) Injectable, Rx Only label on the vial.
The FDA found insanitary conditions at the facility, so the product may be contaminated. Do not use the product until the recall is resolved.
The recall record does not specify a replacement process or remedy.
The recall record does not specify a contact for assistance.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0196-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0196-2023 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.
