Becton Dickinson recalls BD Insyte Autoguard BC Pro Winged IV Catheter (18 GA) due to possible needle failure to retract. Affected units have specific lot numbers and were sold with sterile packaging.
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Becton Dickinson is recalling a specific type of IV catheter because customers reported it might not retract properly after use. This could lead to complications during medical procedures if the needle stays in place.
The catheter needle may not retract correctly after being inserted into a patient's vein. This could cause the needle to remain in place longer than intended, potentially leading to complications like infection or tissue damage.
Healthcare professionals using this catheter for patient IV therapy are most at risk. Patients receiving care with this specific model may also be affected.
Check for the model name 'BD Insyte Autoguard BC Pro Winged Shielded IV Catheter', 18 gauge, 1.16 inches long. The lot number 4298108 or UDI code 382903829446 indicates the recalled units.
Look for the lot number 4298108 or UDI code 382903829446 on the catheter packaging.
Reach out to Becton Dickinson for guidance on next steps if you have the recalled catheter.
The recall indicates a potential issue with needle retraction, so it's recommended to stop using it until further instructions are received.
Check for the lot number 4298108 or UDI code 382903829446 on the packaging.
Contact Becton Dickinson for specific instructions on how to handle the recalled catheter.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2003-2025 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2003-2025 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.
