NavaClick Syringe (Lineage Biomedical) – Incorrect GTIN (2024)
Incorrect GTIN number printed on product carton may cause labeling confusion.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
NavaClick Syringe and Needle, Model Number LIN02
Brand
LINEAGE BIOMEDICAL, INC
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Product Level Labeling Full UDI: (01)00860009080522(17)250416(10)24107. Packaging Carton Level Labeling Full UDI: (01)208600090805(17)250416(10)24107
LINEAGE BIOMEDICAL, INC is recalling NavaClick Syringe and Needle, Model Number LIN02 due to Incorrect GTIN number on carton.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect GTIN number on carton.
Recommended Action
Per FDA guidance
Lineage Biomedical notified consignees via UPS letter on 07/12/2024. The letter instructed consignees to relabel the product with the updated UDI barcode or return inventory on hand for replacement. Additionally, consignees were asked to acknowledge receipt of the notification.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026