Becton Dickinson recalls BD Insyte Autoguard Winged IV catheters due to possible needle failure to retract. Affected units have specific model and lot numbers. Consumers should contact for remedy.
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Becton Dickinson is recalling certain BD Insyte Autoguard Winged IV catheters because the needle might not retract properly. This could lead to complications during medical procedures if the catheter becomes stuck.
The catheter needle may not retract quickly enough or at all when used, potentially causing the needle to remain in the patient's vein. This could lead to complications like infection or improper medication delivery.
Healthcare professionals using the catheter for patient IV therapy are most at risk. Patients receiving IV treatments with this specific catheter model may also be affected.
Check for the model name 'BD Insyte Autoguard Winged, Shielded IV Catheter, 20 GA x 1.00 in (1.1 x 25 mm) 65mL/min, STERILEEO,RxOnly'. Lot numbers include 4282452 or UDI: 382903815333.
Identify the model and lot number on the catheter packaging or label.
Reach out to Becton Dickinson for specific remedy instructions based on your product details.
The recall indicates a potential issue with needle retraction, so it's recommended to stop using the affected catheters until a remedy is provided.
Check for the model name 'BD Insyte Autoguard Winged, Shielded IV Catheter, 20 GA x 1.00 in (1.1 x 25 mm) 65mL/min, STERILEEO,RxOnly' and lot number 4282452 or UDI: 382903815333.
Contact Becton Dickinson directly for specific remedy instructions based on your product details.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2001-2025 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2001-2025 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.
