🔍 RecallPedia

Panacea Air Pro Mattress Control Unit, Model: Platinum 5000, US Model Number 5000. Use with alternating pressure air flotation mattress.

Class I - Dangerous
🏥 Medical Devices Recalled: July 11, 2016 American National Mfg Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Serial No. 9500051 sequential to 9500300.
  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:
American National Mfg Inc
Reason for Recall:
The Panacea Air Pro Mattress Control Unit is being recalled due to a firmware problem, which may result in the device not having the firmness range required.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Panacea Air Pro Mattress Control Unit, Model: Platinum 5000, US Model Number 5000. Use with alternating pressure air flotation mattress.

Product Codes/Lot Numbers:

Serial No. 9500051 sequential to 9500300.

Distribution:

Distributed in: US, WI, OH, IL, TX, AZ, MD, IA, PA, CO, WA, ID, MN, LA, WY, MS

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2605-2016