Centur: Catheter Securement System Recall - Iodine Assay Issue

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Recalling firmCenturion Medical Products Corporation100 Centurion Way, N/A · Williamston, MI 48895-9086

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Centurion Medical is recalling their Catheter Securement System (CSS490) because the PVP Prep Pad in the Convenience Kit doesn't meet the iodine assay level needed for a 36-month shelf life. This could lead to the product not working properly over time.

Why it’s dangerous

The PVP Prep Pad in the Convenience Kit doesn't meet the required iodine assay level for the 36-month shelf life. This means the pad might not function properly over time, potentially affecting catheter security.

Who’s affected

Healthcare professionals using the Catheter Securement System (CSS490) with lot codes 2016022290 or 2017071790 are likely affected. Patients receiving catheter care from these products may be at risk if the product fails.

How to tell if you have this one

Check for the Catheter Securement System (CSS490) with lot codes 2016022290 or 2017071790. The product is sold by Centurion Medical.

Brand
Centurion Medical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Lot Code
Look for lot codes 2016022290 or 2017071790 on the Catheter Securement System (CSS490) packaging.

✎ GovInfoNow

Questions people ask

What is the specific problem with the PVP Prep Pad?

The PVP Prep Pad does not meet the iodine assay level required to support a 36-month shelf life.

How can I tell if my product is affected?

Check for lot codes 2016022290 or 2017071790 on the Catheter Securement System (CSS490).

What should I do if I have the affected product?

The recall record does not specify a remedy, so contact Centurion Medical for guidance.

Take action

Contact Centurion Medical

We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1083-2018 — Centurion Medical Centurion Medical

Hello,

I own a Centurion Medical that is covered by recall Z-1083-2018 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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Where this comes from

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.

Official source: FDA Recall #Z-1083-2018 (October 23, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1083-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 31, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Centurion Medical Products Corporation recalls CATHETER SECUREMENT SYSTEM

Lower-risk recall