🔍 RecallPedia

DERMLITE DL4W, REF: DL4W, Rx Only MD, CE

Class I - Dangerous
🏥 Medical Devices Recalled: March 20, 2023 DermLite Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot # 7654, serial numbers DL4WGXXXX & DL4WBXXXX (1304-1353 and 1504); UDI-DI: (01) 0 8559970
  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:
DermLite LLC
Reason for Recall:
Incorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

DERMLITE DL4W, REF: DL4W, Rx Only MD, CE

Product Codes/Lot Numbers:

Lot # 7654, serial numbers DL4WGXXXX & DL4WBXXXX (1304-1353 and 1504); UDI-DI: (01) 0 8559970

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1506-2023