Aliquot Delivery Kit (Syringe and Plunger); for use in open and percutaneous procedures to facilitate placement of bone cement in weakened or diminished bone

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    All lots, Model Number of device: 2090-0501, 2090-0502, 2090-0504, 2090-0505
  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.

โš ๏ธ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Orthovita, Inc., dBA Stryker Orthobiologics.
Reason for Recall:
Two isolated instances of holes in the outer header bag component of the double barrier sterile packaging configuration
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Aliquot Delivery Kit (Syringe and Plunger); for use in open and percutaneous procedures to facilitate placement of bone cement in weakened or diminished bone

Product Codes/Lot Numbers:

All lots, Model Number of device: 2090-0501, 2090-0502, 2090-0504, 2090-0505

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2772-2015

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