🔍 RecallPedia

ElectroMist product codes: 36-3310-25 - Product Usage: Electrode conductivity spray solution.

Class I - Dangerous
🏥 Medical Devices Recalled: June 19, 2019 Pharmaceutical Innovations Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot # 060714-25, 080614-25, 101515-25, 070116-25, 072816-25A, 072816-25, 021317-25, 010118-25,102018-25.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Pharmaceutical Innovations, Inc.
Reason for Recall:
Potential for failed stability antimicrobial effectiveness testing.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

ElectroMist product codes: 36-3310-25 - Product Usage: Electrode conductivity spray solution.

Product Codes/Lot Numbers:

Lot # 060714-25, 080614-25, 101515-25, 070116-25, 072816-25A, 072816-25, 021317-25, 010118-25,102018-25.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1969-2019

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Pharmaceutical Innovations

Class I - Dangerous

The firm registered the product as a Class I device, but has since been informed by FDA that the device is not Class I and requires a 510(k) submission.

Aug 13, 2020 Other Medical Devices Nationwide View Details →