Pharmacy Innovations recalls 10ml vials of phosphatidylcholine/deoxycholic acid injectable due to FDA finding insanitary conditions at manufacturing facility.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling a specific injectable medication product because FDA inspections found unsanitary conditions at their manufacturing facility. This means the product may not be sterile, which could cause serious infections if used.
The FDA found unsanitary conditions at the manufacturing facility, which means the product may not be sterile. If used, this could lead to serious infections or other health complications.
People with prescriptions for this injectable medication from Pharmacy Innovations. Those using the product for medical treatments are at highest risk.
Check for the product name 'Phosphatidylcholine/Deoxycholic Acid (10ML Vial) 50MG/50MG/ML (5%/5%) Injectable' with the manufacturer Pharmacy Innovations. The product was sold in Erie, PA.
Discard the product immediately as it may not be sterile and could cause serious infections.
No, the FDA found unsanitary conditions at the manufacturing facility, so the product may not be sterile and could cause serious infections.
Check for the product name 'Phosphatidylcholine/Deoxycholic Acid (10ML Vial) 50MG/50MG/ML (5%/5%) Injectable' with the manufacturer Pharmacy Innovations.
Discard the product immediately as it may not be sterile and could cause serious infections.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0230-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0230-2023 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.
