Becton Dickinson recalls BD Connecta Plus1 360 Blue Blend infusion devices with catalog number 394911 (OUS) due to potential leakage at the stopcock housing, which could cause treatment delays, contamination, or under-dosing.
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under dosing/under infusion, contamination and/or air ingress.
Becton Dickinson is recalling BD Connecta Plus1 360 Blue Blend infusion devices with catalog number 394911 (OUS) because they may leak at the stopcock housing. This could lead to treatment delays, under-dosing, contamination, or exposure to biohazardous materials. Affected users should stop using the device immediately to prevent potential health risks.
The stopcock housing in these infusion devices may leak, causing treatment interruptions, under-dosing of medication, contamination of the infusion, or exposure to biohazardous materials. This leakage could occur during normal use and affect patient safety.
Patients using BD Connecta Plus1 360 Blue Blend infusion devices with catalog number 394911 (OUS) are most at risk. Healthcare providers administering these devices may also be affected.
Check for the catalog number 394911 (OUS) on the device. The lot number and expiration date are 1061512 and 2/29/2024, respectively.
Inspect the stopcock housing for signs of leakage or damage.
Reach out to Becton Dickinson for further guidance on the recall.
The catalog number is 394911 (OUS).
Leakage could cause treatment delays, under-dosing, contamination, or exposure to biohazardous materials.
Look for the catalog number 394911 (OUS) on the device. The lot number and expiration date are 1061512 and 2/29/2024, respectively.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-1437-2022 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-1437-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
