Pharmaceutical Innovations recalls ElectroMist electrode conductivity spray solution (product codes 36-3310-04) due to potential failed antimicrobial effectiveness testing. Affected lots include 030215-04, 011716-04, 072816-04, 071618-04, 080117-04.
Potential for failed stability antimicrobial effectiveness testing.
Pharmaceutical Innovations is recalling ElectroMist electrode conductivity spray solution (product code 36-3310-04) 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 could lead to contamination in medical environments if the product is used for electrode conductivity purposes.
Healthcare professionals and medical facilities using ElectroMist electrode conductivity spray solution for medical purposes are most likely affected. The risk is low for general consumers who do not use this product.
Check for product code 36-3310-04 on the label. Affected lots include 030215-04, 011716-04, 072816-04, 071618-04, and 080117-04.
Look for product code 36-3310-04 on the label to confirm if it's affected.
The recall applies to medical facilities using ElectroMist for electrode conductivity. Home users are not affected as this product is not intended for general home use.
The recall record does not specify a remedy, so no action is required beyond checking if you have the affected product code.
Check the product code on the label. Affected lots include 030215-04, 011716-04, 072816-04, 071618-04, and 080117-04.
We’ve drafted a message you can send Pharmaceutical Innovations to request your refund or repair — edit it as you like.
Subject: Recall Z-1971-2019 — Pharmaceutical Innovations Pharmaceutical Innovations Hello, I own a Pharmaceutical Innovations that is covered by recall Z-1971-2019 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.
