🔍 RecallPedia

Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense Product Usage: Automated anesthesia cart that monitors and controls the dispensing of medications, narcotics and supplies during surgical procedures.

Class I - Dangerous
🏥 Medical Devices Recalled: July 22, 2013 MCKESSON TECHNOLOGIES Diagnostic Equipment Nationwide

What Should You Do?

  1. Check if you have this product:
    Model Number (software version) 8.0.2 & 8.0.1 with RapiDispense
  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:
MCKESSON TECHNOLOGIES INC
Reason for Recall:
The firm issued a clinical alert after users reported an issue where the Anesthesia-Rx system was interrupted ANF became temporarily unavailable during use.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense Product Usage: Automated anesthesia cart that monitors and controls the dispensing of medications, narcotics and supplies during surgical procedures.

Product Codes/Lot Numbers:

Model Number (software version) 8.0.2 & 8.0.1 with RapiDispense

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2089-2013

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