Centurion Medical recalls CAP Bundle Kit DYNDC2137 due to potential fluid droplets separating after disconnection. Affected units sold in 2018. No remedy stated 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 a specific medical kit (DYNDC2137) because it might release fluid droplets when disconnected. This could pose a risk during medical procedures. The recall is for kits sold starting in 2018.
The BD MaxZeroNeedleless Connector in the kit may release fluid droplets when disconnected. This could lead to contamination or exposure during medical procedures. The risk is specific to the connector's design when it's removed from the device.
Healthcare workers using this kit for medical procedures are most at risk. Patients receiving care with this kit could also be affected.
Check for the model number DYNDC2137 on the kit packaging. This recall applies to kits sold starting in 2018.
Look for the model number DYNDC2137 on the kit packaging to confirm if it is affected.
The recall states there is a potential for fluid droplets to separate after disconnection, but no specific remedy is stated. The risk is considered low.
The recall applies to kits sold starting in 2018.
The official notice does not specify a remedy, so no action is required beyond checking if you have the affected model.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0087-2020 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-0087-2020 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.
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.
