Becton Dickinson recalls BD Nexiva IV catheter systems due to non-sterile packaging. This could lead to infections if used without proper sterility. Affected units have specific batch numbers and model numbers.
There is a breach in the product packaging that renders the product non-sterile.
Becton Dickinson is recalling BD Nexiva IV catheter systems because the packaging may be breached, making the product non-sterile. Using these catheters could lead to infections if not properly sterilized.
The product packaging has a breach that makes the catheter non-sterile. If the catheter is used without proper sterilization, it could lead to infections in patients or healthcare workers.
Healthcare professionals and patients using BD Nexiva IV catheter systems for short-term blood sampling, monitoring, or fluid administration. Those with specific batch numbers are most at risk.
Check for the model number 383536 and batch numbers listed: 1193055, 1166273, 1188953. These units were sold with specific dates and lot numbers.
Look for the model number 383536 and batch numbers 1193055, 1166273, or 1188953 on the packaging.
The packaging has a breach that renders the product non-sterile, which could lead to infections if used without proper sterilization.
Check the model number and batch numbers on the packaging. If it matches the recalled units, stop using it and contact Becton Dickinson for further instructions.
The recall record does not mention a remedy or fix. Affected units should be checked and disposed of if they match the recalled batch numbers.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-0306-2022 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-0306-2022 from Becton Dickinson. 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.
