Pharmacy Innovations recalls LidoCaine-PF 5% (5ml vial) injectable due to FDA finding insanitary conditions at manufacturing facility. This may cause infections if used.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling LidoCaine-PF 5% (5ml vial) injectable products because FDA inspections found unsanitary conditions at their Erie, PA facility. Using these products could lead to infections if they are not sterile.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility in Erie, PA. This means the injectable products might not be sterile, which could cause infections if used.
People who have prescription LidoCaine-PF 5% (5ml vial) injectable products from Pharmacy Innovations in Erie, PA. Those with medical conditions requiring injections are most at risk.
Check for LidoC: 5% (5ml vial) injectable products labeled as Pharmacy Innovations, manufactured in Erie, PA. The recall was issued on October 11, 2022, and the product was sold until November 8, 2022.
Look for the product name LidoCaine-PF 5% (5ml vial) injectable with Pharmacy Innovations label from Erie, PA.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility in Erie, PA, which may mean the product is not sterile.
The recall record does not mention any remedy or fix for this product.
Check for LidoCaine-PF 5% (5ml vial) injectable products labeled as Pharmacy Innovations from Erie, PA, sold between October 11, 2022, and November 8, 2022.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0218-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0218-2023 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.
