🔍 RecallPedia

CAIRE Liberator 45, MODEL 13261699, Liquid Oxygen System Unit

Class I - Dangerous
🏥 Medical Devices Recalled: October 10, 2022 Caire Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI/DI M766132616990, Serial Numbers: CBB3022310887, CBB3022310888, CBB3022310852, CBB3022310823, CBB3022310792, CBB3022310843, CBB3022310844, CBB3022310827, CBB3022310842, CBB3022310845
  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:
Caire, Inc.
Reason for Recall:
An audit discovered some inconsistencies in weld penetration on the longitudinal weld seam on the inner bottle of the device on some of the units.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

CAIRE Liberator 45, MODEL 13261699, Liquid Oxygen System Unit

Product Codes/Lot Numbers:

UDI/DI M766132616990, Serial Numbers: CBB3022310887, CBB3022310888, CBB3022310852, CBB3022310823, CBB3022310792, CBB3022310843, CBB3022310844, CBB3022310827, CBB3022310842, CBB3022310845

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0336-2023

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