🔍 RecallPedia

NavaClick Syringe and Needle, Model Number LIN02

Class I - Dangerous
🏥 Medical Devices Recalled: July 12, 2024 LINEAGE BIOMEDICAL Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    Product Level Labeling Full UDI: (01)00860009080522(17)250416(10)24107. Packaging Carton Level Labeling Full UDI: (01)208600090805(17)250416(10)24107
  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:
LINEAGE BIOMEDICAL, INC
Reason for Recall:
Incorrect GTIN number on carton.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

NavaClick Syringe and Needle, Model Number LIN02

Product Codes/Lot Numbers:

Product Level Labeling Full UDI: (01)00860009080522(17)250416(10)24107. Packaging Carton Level Labeling Full UDI: (01)208600090805(17)250416(10)24107

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2535-2024