Lineage Biomedical recalls NavaClick Syringe Model LIN02 due to incorrect GTIN number on carton. This labeling issue may cause confusion in product identification.
Incorrect GTIN number on carton.
Lineage Biomedical is recalling Nava:Click syringes and needles with model number LIN02 because the carton has an incorrect GTIN number. This labeling error could lead to confusion about which product is being used, potentially causing mistakes in medical procedures.
The incorrect GTIN number on the carton can cause confusion about which syringe and needle product is being used. This labeling error may lead to mistakes in medical procedures if the wrong product is selected.
Healthcare professionals and patients who use NavaClick syringes with model number LIN02 are affected. Those most at risk are individuals who rely on precise product identification for medical treatments.
Check for the model number LIN02 on the syringe and needle packaging. The carton should have the GTIN number (01)208600090805(17)250416(10)24107, but the current labeling is incorrect.
Verify the carton has the correct GTIN number (01)208600090805(17)250416(10)24107. If it does not, contact Lineage Biomedical for guidance.
Lineage Biomedical is recalling NavaClick syringes and needles with model number LIN02 due to an incorrect GTIN number on the carton.
Check for the model number LIN02 on the syringe and needle packaging. The carton should have the GTIN number (01)208600090805(17)250416(10)24107, but the current labeling is incorrect.
Contact Lineage Biomedical for guidance on how to handle the product if the carton does not have the correct GTIN number.
We’ve drafted a message you can send Lineage Biomedical to request your refund or repair — edit it as you like.
Subject: Recall Z-2535-2024 — Lineage Biomedical Lineage Biomedical Hello, I own a Lineage Biomedical that is covered by recall Z-2535-2024 from Lineage Biomedical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
