Becton Dickinson recalls BD Connecta Plus3 White Blend OEM (sterile, bulk) Catalog No. 395214 (OUS) due to potential leakage at the stopcock housing, which may 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 Plus3 White Blend OEM (sterile, bulk) products with Catalog No. 395214 (OUS) because they may leak at the stopcock housing. This could lead to treatment interruptions, contamination, or incorrect dosing of medical fluids.
The stopcock housing may leak, causing treatment interruptions, exposure to infusate and biohazardous materials, under-dosing, or air entering the system. This could lead to incorrect medication delivery or infection risks.
Healthcare professionals using this product for medical infusions are most at risk. Patients receiving treatments with this device could experience delays or contamination if the product leaks.
Check for the product name 'BD Connecta Plus3 White Blend OEM (sterile, bulk)' with Catalog No. 395214 (OUS). Lot numbers include 1127328.
Identify the product by its catalog number (395214) and lot number (1127328) to confirm if it is affected.
The recall indicates a potential leakage risk, so it is not recommended for use until the remedy is applied. However, the remedy is not specified in the record.
The recall record does not specify a remedy, so contact Becton Dickinson for guidance on next steps.
Check for the catalog number 395214 (OUS) and lot number 1127328 on the product label.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-1439-2022 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-1439-2022 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.
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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.
