Centurion Medical recalls circumcision trays with specific lot codes due to PVP prep pad not meeting iodine assay levels for 36-month shelf life. Affected units may have reduced effectiveness.
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Centurion Medical is recalling circumcision trays with certain lot codes because the PVP prep pad inside doesn't meet the required iodine levels to stay effective for 36 months. This could mean the pad doesn't work properly during procedures.
The PVP prep pad in the tray doesn't meet the iodine assay level needed to last 36 months. This could mean the pad becomes less effective over time, potentially reducing its ability to properly prepare the skin during circumcision procedures.
People who purchased circumcision trays with the listed lot codes from the provided dates. Healthcare providers using these trays for medical procedures are most at risk.
Check the lot code on the tray, which is listed in the provided codes (e.g., 2015081790, 2015111390). These codes were used between August 2015 and May 2017 for specific models.
Look for the lot code on the tray, which should match one of the listed codes (e.g., 2015081790, 2015111390).
The PVP prep pad in the tray does not meet the required iodine assay level to support a 36-month shelf life, which could reduce its effectiveness during procedures.
Check the lot code on the tray against the provided list. If it matches, contact Centurion Medical for guidance.
The recall is due to reduced effectiveness of the prep pad over time, not an immediate safety hazard. No injuries have been reported.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1082-2018 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-1082-2018 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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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.
