🔍 RecallPedia

Aguja de Aspiracion con Profundidad Ajustable Tipo I 16ga x 5 cm- Product Usage: Manual surgical instruments for Bone Marrow Biopsy and Aspiration.

Class I - Dangerous
🏥 Medical Devices Recalled: December 18, 2018 Angiotech (Manan Medical Products, Inc.) Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    Model Number UCIN-16-5, Lot Number LK2L
  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:
Angiotech (Manan Medical Products, Inc.)
Reason for Recall:
Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Aguja de Aspiracion con Profundidad Ajustable Tipo I 16ga x 5 cm- Product Usage: Manual surgical instruments for Bone Marrow Biopsy and Aspiration.

Product Codes/Lot Numbers:

Model Number UCIN-16-5, Lot Number LK2L

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0818-2019

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