Pharmaceutical Innovations recalls ElectroMist electrode conductivity spray solution (product codes 36-3310-60) due to potential failure in antimicrobial effectiveness testing. Affected lots: 051914-60, 101615-60, 021317-60.
Potential for failed stability antimicrobial effectiveness testing.
Pharmaceutical Innovations is recalling ElectroMist electrode conductivity spray solution (product code 36-3310-60) because it may not work properly to prevent contamination. This could lead to infections if used in medical settings.
The spray solution may fail antimicrobial effectiveness testing, meaning it could not properly prevent contamination. This could lead to infections if used in medical environments where sterile conditions are critical.
Healthcare professionals and medical facilities using ElectroMist for electrode conductivity testing are most at risk. The recall affects specific product lots sold between 2019 and 2017.
Check for product code 36-3310-60 on the ElectroMist electrode conductivity spray solution. Affected lots include 051914-60, 101615-60, and 021317-60.
Look for lot numbers 051914-60, 101615-60, or 021317-60 on the ElectroMist electrode conductivity spray solution.
The recall states potential failure in antimicrobial effectiveness testing, but does not specify that the product is dangerous if used correctly.
Check for product code 36-3310-60 and lot numbers 051914-60, 101615-60, or 021317-60.
The recall does not specify a stop-use instruction, so users can continue using it if they have a different lot number.
We’ve drafted a message you can send Pharmaceutical Innovations to request your refund or repair — edit it as you like.
Subject: Recall Z-1970-2019 — Pharmaceutical Innovations Pharmaceutical Innovations Hello, I own a Pharmaceutical Innovations that is covered by recall Z-1970-2019 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.
