🔍 RecallPedia

Sara Plus Active Floor Lift

Class I - Dangerous
🏥 Medical Devices Recalled: April 5, 2022 ARJOHUNTLEIGH POLSKA Sp. z.o.o. Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    Model Numbers: HEP0001, HEP0001-AU, HEP0001-BR, HEP0001-CN, HEP0001-JP, HEP0001-UK, HEP0001-US, HEP1001, HEP1001-AU, HEP1001CON4869, HEP1001-US, HEP2001, HEP2001-BR, HEP2001-CN, HEP2001-UK
  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:
ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Reason for Recall:
The device may emit smoke or ignite.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Sara Plus Active Floor Lift

Product Codes/Lot Numbers:

Model Numbers: HEP0001, HEP0001-AU, HEP0001-BR, HEP0001-CN, HEP0001-JP, HEP0001-UK, HEP0001-US, HEP1001, HEP1001-AU, HEP1001CON4869, HEP1001-US, HEP2001, HEP2001-BR, HEP2001-CN, HEP2001-UK

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1098-2022

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ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Class I - Dangerous

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