Becton Dickinson recalls BD Insyte Autoguard BC Winged IV catheters with possible slow or failed needle retraction due to customer complaints. Affected units have specific model and lot numbers.
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 BC Winged IV catheters because customers reported the needle may retract slowly or fail to retract. This could lead to complications during IV treatments if the needle doesn't move properly.
The catheter's needle may retract slowly or fail to retract during use, which could cause the needle to stay in place longer than intended. This might lead to complications like infection or tissue damage if the needle doesn't move properly.
Healthcare professionals and patients using the recalled catheters are affected. Those receiving IV treatments with the specific model are most at risk.
Check for the model: BD Insyte Autoguard BC Winged, Shielded IV Catheter with Blood Control Technology, 20GA x 1.00 in (1.1x25 mm). Look for lot number 4222721 or UDI 382903826339 on the packaging.
Look for the model number and lot number on the packaging to confirm if it's affected.
Reach out to your healthcare provider for guidance on alternative catheters or safe usage.
The recall states there is a possibility of slow or failed needle retraction, so it's not recommended for use without checking the recall status.
Check for the model: BD Insyte Autoguard BC Winged, Shielded IV Catheter with Blood Control Technology, 20GA x 1.00 in (1.1x25 mm) and lot number 4222721 or UDI 382903826339.
Contact your healthcare provider for guidance on alternative catheters or safe usage options.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2000-2025 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2000-2025 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.
