🔍 RecallPedia

MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U.

Class I - Dangerous
🏥 Medical Devices Recalled: August 30, 2024 MEDLINE INDUSTRIES, LP - Northfield Patient Monitors Nationwide

What Should You Do?

  1. Check if you have this product:
    GTIN 00888277704049. Lot Numbers: L230480007, L230880007, L231080007, L231280007, L240380007
  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:
MEDLINE INDUSTRIES, LP - Northfield
Reason for Recall:
It has been determined that certain Blood Pressure Monitors containing a faulty microchip have failed to power on or have shown display screen issues after the initial few uses, as well as overheating at times making the unit warm to the touch.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U.

Product Codes/Lot Numbers:

GTIN 00888277704049. Lot Numbers: L230480007, L230880007, L231080007, L231280007, L240380007

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0033-2025

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