🔍 RecallPedia

PrepIT Q2A Kit, Model PT-Q2A-96 containing component reagent AG (PT-QAG-96) 1.4mL and ST (PT-QST-96) 2.9mL - Product Usage: used for the removal of SDS and other inhibitors from samples collected using DNA Genotek oral sample collection kits.

Class I - Dangerous
🏥 Medical Devices Recalled: June 24, 2020 DNA Genotek Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot PT-Q2A WE11
  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:
DNA Genotek Inc.
Reason for Recall:
Reagents were shipped to customers after the Use by data indicated on its labeling.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

PrepIT Q2A Kit, Model PT-Q2A-96 containing component reagent AG (PT-QAG-96) 1.4mL and ST (PT-QST-96) 2.9mL - Product Usage: used for the removal of SDS and other inhibitors from samples collected using DNA Genotek oral sample collection kits.

Product Codes/Lot Numbers:

Lot PT-Q2A WE11

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-3004-2020

Related Recalls