Pharmaceutical Innovations recalls Alpha Conducting solution (product codes 3310-15 ACS) due to potential failure in antimicrobial effectiveness testing. Affected lots from 081914-15 to 102018-15.
Potential for failed stability antimicrobial effectiveness testing.
Pharmaceutical Innovations is recalling Alpha Conducting solution product codes 3310-15 ACS because it may not work properly to prevent contamination. This could lead to infections if used in medical settings.
The solution may fail antimicrobial effectiveness testing, meaning it could not properly prevent contamination. This poses a risk of infection if used in medical settings where sterile conditions are critical.
Healthcare professionals and medical facilities using the Alpha Conducting solution for electrode conductivity testing are most at risk. The product is intended for medical use, so users must check if they have the affected lots.
Check for product codes 3310-15 ACS on the label. Affected lots include 081914-15 through 102018-15. The product is an electrode conductivity spray solution used in medical settings.
Look for product code 3310-15 ACS on the label to confirm if it is affected.
The recall states there is a potential for failed antimicrobial effectiveness testing, so it may not be safe for medical use. Affected lots should not be used.
The recall does not specify a remedy, so contact the manufacturer directly for guidance.
Affected lots are 081914-15, 111715-15, 070116-15, 020117-15, 080117-15, 010118-15, 041618-15, 041618A-15, 071618-15, and 102018-15.
We’ve drafted a message you can send Pharmaceutical Innovations to request your refund or repair — edit it as you like.
Subject: Recall Z-1968-2019 — Pharmaceutical Innovations Pharmaceutical Innovations Hello, I own a Pharmaceutical Innovations that is covered by recall Z-1968-2019 from Pharmaceutical 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.
