LINEAGE BIOMEDICAL, INC: Device Recall
Recall #Z-2535-2024 · 07/12/2024
Class III: Low Risk
Recall Details
- Recall Number
- Z-2535-2024
- Classification
- Class III
- Product Type
- Device
- Recalling Firm
- LINEAGE BIOMEDICAL, INC
- Status
- Ongoing
- Date Initiated
- 07/12/2024
- Location
- Stuart, FL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 215 cartons (containing 50 pouches each)
Reason for Recall
Incorrect GTIN number on carton.
Product Description
NavaClick Syringe and Needle, Model Number LIN02
Distribution Pattern
US Nationwide distribution in the states of Michigan and South Carolina.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.