🔍 RecallPedia

Trilogy 100, Trilogy 200, Trilogy O2, Trilogy 202, Trilogy EC, Garbin, Garbin Plus Trilogy 100, Trilogy 200, Garbin, Garbin plus provides continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilation.

Class I - Dangerous
🏥 Medical Devices Recalled: January 18, 2016 Philips Respironics Patient Monitors Nationwide

What Should You Do?

  1. Check if you have this product:
    11 digit S/N begginning with GV or TV; also TGY1D01463
  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:
Philips Respironics
Reason for Recall:
Software Issue
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Trilogy 100, Trilogy 200, Trilogy O2, Trilogy 202, Trilogy EC, Garbin, Garbin Plus Trilogy 100, Trilogy 200, Garbin, Garbin plus provides continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilation.

Product Codes/Lot Numbers:

11 digit S/N begginning with GV or TV; also TGY1D01463

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1065-2016

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