Becton Dickinson recalls BD Connecta White 360 Shelf 100Ea (Catalog No. 395000) due to potential leakage at the stopcock housing, which may cause treatment delays, contamination, or under-dosing. Affected units have specific lot numbers and expiration dates.
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 White 360 Shelf 100Ea infusion systems because they may leak at the stopcock housing. This could lead to treatment delays, contamination, or incorrect dosing of medical fluids. Patients using these devices should contact the manufacturer for guidance.
The stopcock housing in these infusion systems may leak, causing treatment delays, exposure to biohazardous materials, under-dosing of fluids, or air entering the system. This could lead to incorrect medication delivery or contamination risks.
Patients using BD Connecta White 360 Shelf 100Ea infusion systems with specific lot numbers and expiration dates are affected. Healthcare providers administering treatments with these devices are most at risk.
Check for the catalog number 395000 (OUS) on the product label. Affected units have specific lot numbers: 1120604 (exp 3/31/2024), 1098929 (exp 3/31/2024), 1123643 (exp 4/30/2024), and 1063423 (exp 2/29/2024).
Verify the catalog number 395000 (OUS) and lot numbers listed above to confirm if your device is affected.
The stopcock housing may leak, causing treatment delays, contamination, or under-dosing of medical fluids.
Check the product label for the catalog number 395000 (OUS) and lot numbers to determine if it's affected. Contact Becton Dickinson for further instructions.
The recall states potential for treatment delays and contamination, but does not mention serious injury risks. The hazard level is low risk.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-1438-2022 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-1438-2022 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.
