Centurion Medical recalls specific instrument trays due to PVP Prep Pad failing iodine assay standards, risking shelf life and safety. Affected models include 75121, 75175, 71435, etc. with certain lot codes.
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 specific general purpose instrument trays because the PVP Prep Pad inside them doesn't meet iodine assay requirements needed for a 36-month shelf life. This could mean the pads degrade faster than intended, potentially affecting medical procedures.
The PVP Prep Pad in the trays was received by a supplier and doesn't meet the required iodine assay level. This means the pad may degrade faster than intended, potentially compromising the tray's shelf life and safety for medical use.
Healthcare professionals using the recalled instrument trays are most at risk, particularly those in settings where these trays are used for medical procedures.
Check for lot codes listed in the recall: 2017071990, 2016110990, 2016040790, and other codes listed in the product description. The affected models include 75121, 75175, 71435, 75455, 75690, SR245.
Look for lot codes such as 2017071990, 2016110990, or others listed in the recall notice to identify affected units.
The PVP Prep Pad in the recalled instrument trays was received by a supplier and does not meet the iodine assay level required for a 36-month shelf life.
The affected models include 75121, 75175, 71435, 75455, 75690, and SR245 with specific lot codes listed in the recall notice.
The recall does not specify a remedy, so no action is required beyond checking if your product has the listed lot codes.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1080-2018 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-1080-2018 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.
