🔍 RecallPedia

Capnostream20 (INTL) M REFURBISHED, CS78654

Class I - Dangerous
🏥 Medical Devices Recalled: July 31, 2018 Oridion Medical 1987 Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    B300001467 B300001028 B300001013 B300001063 B300001239 B300001299 B300001432 B300001465 B300001233 B500001792 B500001690
  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:
Oridion Medical 1987 Ltd.
Reason for Recall:
The date/time, nurse call and alarm settings of the bedside patient monitors may reset to the factory default settings when the monitor is powered off.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Capnostream20 (INTL) M REFURBISHED, CS78654

Product Codes/Lot Numbers:

B300001467 B300001028 B300001013 B300001063 B300001239 B300001299 B300001432 B300001465 B300001233 B500001792 B500001690

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0052-2019

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Oridion Medical 1987

Class I - Dangerous

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Class I - Dangerous

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