Becton Dickinson recalls BD Cathena Safety IV catheters with potential safety shield failure, risking needle exposure during use. Affected units include specific model and lot numbers.
There is the potential that the safety shield may not properly engage on IV catheters. The needle can pull through the safety shield and disconnect from the needle safety shield leaving the contaminated needle point exposed.
Becton Dickinson is recalling certain BD Cathena Safety IV catheters because the safety shield might not stay securely attached. If the shield fails, the needle could become exposed and contaminated, posing a risk of infection or injury.
The safety shield may not properly engage with the IV catheter, allowing the needle to pull through and disconnect. This exposes the contaminated needle tip, increasing the risk of infection or injury.
Healthcare professionals and patients using the recalled catheters are most at risk. The specific model and lot numbers are critical for identification.
Check for the model: BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA, 1.00 IN, 1.1 x 25 mm, 64 mL/min. The lot number is 2238464 or UDI-DI: (01)00382903868629.
Ensure the safety shield is securely engaged with the catheter before use. If it feels loose, stop using the catheter immediately.
The recall applies to healthcare professionals and patients using the catheters in medical settings.
Check for the model: BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA, 1.00 IN, 1.1 x 25 mm, 64 mL/min. The lot number is 2238464 or UDI-DI: (01)00382903868629.
The recall does not specify a remedy, but you should check the safety shield engagement before use. If it feels loose, stop using the catheter immediately.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-0025-2024 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-0025-2024 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.
