Pharmaceutical Innovations recalls ElectroMist electrode conductivity spray solution (product codes 36-3310-25) due to potential failure in antimicrobial effectiveness testing. Affected units include specific lot numbers from 2014-2018.
Potential for failed stability antimicrobial effectiveness testing.
Pharmaceutical Innovations is recalling ElectroMist electrode conductivity spray solution (product code 36-3310-25) because it may not work properly to prevent microbial growth. This could lead to contamination if the product is used in medical settings.
The product may fail antimicrobial effectiveness testing, meaning it could not properly prevent microbial growth. This risk is specific to medical use where contamination could occur.
Users of ElectroMist electrode conductivity spray solution for medical applications are affected. Healthcare professionals and facilities using the product are most at risk.
Check for product code 36-3310-25 on the ElectroMist electrode conductivity spray solution. Affected lots include 060714-25 through 102018-25, sold between 2014 and 2018.
Look for product code 36-3310-25 on the ElectroMist electrode conductivity spray solution.
The recall states there is a potential for failed antimicrobial effectiveness testing, so it may not prevent microbial growth. The product is not safe for medical use without further verification.
The recall does not specify a remedy, so no action is required beyond checking if you have the affected product code and lot numbers.
Check the product code (36-3310-25) and lot numbers (060714-25 through 102018-25) to see if it matches the affected units.
We’ve drafted a message you can send Pharmaceutical Innovations to request your refund or repair — edit it as you like.
Subject: Recall Z-1969-2019 — Pharmaceutical Innovations Pharmaceutical Innovations Hello, I own a Pharmaceutical Innovations that is covered by recall Z-1969-2019 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.
