Centurion Medical recalls sterile cap change kit DYNDC1946B due to potential fluid droplets separating after disconnection. Affected units sold in 2018-2019. No remedy specified in official notice.
Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Centurion Medical is recalling sterile cap change kits with model DYNDC1946B because fluid droplets might separate from the connector after it's disconnected. This could lead to contamination during medical procedures. The recall affects kits sold between 2018 and 2019.
The BD MaxZeroNeedleless Connector in the kit may release fluid droplets when disconnected. This could cause contamination if the connector is used in medical procedures without proper precautions. The risk is low but requires careful handling.
Healthcare professionals using sterile cap change kits for medical procedures are most at risk. Patients receiving care with these kits could be exposed to potential contamination.
Check for the model number DYNDC1946B on the kit. Kits were sold between 2018 and 2019 with serial numbers starting with 2018101790, 2018092790, or 2019030690.
Look for the model number DYNDC1946B on the sterile cap change kit.
The official recall notice does not specify any remedy.
Kits were sold between 2018 and 2019.
Fluid droplets might separate from the connector after disconnection, potentially causing contamination during medical procedures.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0086-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0086-2020 from Centurion Medical. 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.
