Becton Dickinson recalls BD Insyte Autoguard Winged Shielded IV Catheters due to possible needle failure to retract, risking improper blood draws.
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 IV catheters because the needle might not retract properly, which could lead to improper blood draws or infections. This affects patients receiving IV treatments and healthcare workers using the catheters.
The catheter needle may slow to retract or fail to retract during use, potentially causing improper blood draws or infections. This happens because the needle's mechanism doesn't function correctly in some cases.
Patients receiving IV treatments and healthcare workers using the catheters are most at risk. The recall applies to specific model numbers sold with prescription.
Check for the model: BD Insyte Autoguard Winged Shielded IV Catheter, 22 GA x 1.00 in (0.9 x 25 mm) 35 mL/min, STERILEEO, RxOnly. The recall covers specific lot numbers and UDI codes.
Look for the model number and UDI code on the catheter packaging or label.
Due to customer complaints, the needle may slow to retract or fail to retract, potentially causing improper blood draws or infections.
Check for the model: BD Insyte Autoguard Winged Shielded IV Catheter, 22 GA x 1.00 in (0.9 x 25 mm) 35 mL/min, STERILEEO, RxOnly. The recall covers specific lot numbers and UDI codes.
The recall does not specify a remedy, so contact Becton Dickinson for guidance on next steps.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2006-2025 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2006-2025 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.
