Centurion Medical Products recalls several dressing change kits due to incomplete sterile package seals that may compromise sterility. Affected kits include DYNDC1182B through DYNDC2691 models sold from 2018-2019.
Incomplete seals on the sterile package may compromise the sterility
Centurion Medical Products is recalling multiple dressing change kits and central line trays because their sterile packaging may have incomplete seals. This could allow contamination, risking infection for patients using these medical devices.
Incomplete seals on the sterile packaging could allow contaminants to enter the sterile environment. This might lead to infections if the kits are used without proper sterility.
Healthcare providers and patients using the recalled dressing change kits and central line trays. Those most at risk are individuals with medical devices requiring sterile procedures.
Check for product model numbers starting with DYNDC1182B through DYNDC2691. These kits were sold between February 2018 and June 2019 with specific lot numbers listed in the recall notice.
Look for model numbers starting with DYNDC1182B through DYNDC2691 on the packaging or label.
The recall is due to incomplete seals on the sterile packaging, which could compromise sterility and lead to contamination risks.
Affected models include DYNDC1182B through DYNDC2691, sold between February 2018 and June 2019 with specific lot numbers listed in the recall notice.
No, the recall does not require immediate discontinuation. However, you should check if your kit is affected and follow the provided steps.
We’ve drafted a message you can send Centurion to request your refund or repair — edit it as you like.
Subject: Recall Z-1049-2020 — Centurion Centurion Hello, I own a Centurion that is covered by recall Z-1049-2020 from Centurion. 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.
