Becton Dickinson recalls certain BD Insyte Autoguard Shielded IV Catheters due to potential slow or failed needle retraction, which may cause complications during infusion therapy.
Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
Becton Dickinson is recalling specific IV catheters that may have a needle that doesn't retract properly, potentially causing complications during medical treatments. This affects patients receiving intravenous therapy who use these catheters.
The catheter needle may retract slowly or fail to retract during use, which could lead to complications like dislodgement or improper blood flow. This risk is specific to the catheter's design and function during medical procedures.
Patients using the recalled IV catheters for infusion therapy are most at risk. Healthcare providers who administer these catheters may also be affected.
Check for the model name 'BD Insyte Autoguard Shielded IV Catheter, 18 GA x 1.16 in (1.3 x 30 mm) 95 mL/min, STERILEEO, RxOnly' with lot number 4312025 or UDI 00382903825448.
Identify the product by checking the lot number (4312025) or unique device identifier (UDI: 00382903825448) on the catheter packaging.
The recall is due to customer complaints about the catheter needle potentially retracting slowly or failing to retract, which could cause complications during infusion therapy.
Look for the model name 'BD Insyte Autoguard Shielded IV Catheter, 18 GA x 1.16 in (1.3 x 30 mm) 95 mL/min, STERILEEO, RxOnly' with lot number 4312025 or UDI 00382903825448.
The recall does not specify a remedy, so contact Becton Dickinson directly 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-2005-2025 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2005-2025 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.
