Centurion recalls ENT SNUFFER KIT Y due to incomplete sterile package seals that may compromise sterility. Affected units sold in 2019 with lot number 2019011490.
Incomplete seals on the sterile package may compromise the sterility
Centurion is recalling its ENT SNUFFER KIT Y product because the sterile packaging may not seal properly, risking contamination. This could lead to infections if the kit is used without proper sterility.
The sterile packaging may not seal completely, allowing contaminants to enter the kit. This could lead to infections if the kit is used without proper sterility.
Patients using ENT SNUFFER KIT Y for nasal procedures. Those with medical conditions requiring sterile equipment may be at higher risk.
Check for the product name 'ENT SNUFFER KIT Y' with lot number 2019011490. This kit was sold in 2019.
Inspect the sterile packaging for any signs of incomplete seals.
The recall indicates potential sterility risks, so it is not recommended for use until the issue is resolved.
Look for the product name 'ENT SNUFFER KIT Y' with lot number 2019011490, sold in 2019.
The recall does not specify a remedy, so check the packaging for incomplete seals and contact Centurion for guidance.
We’ve drafted a message you can send Centurion to request your refund or repair — edit it as you like.
Subject: Recall Z-1091-2020 — Centurion Centurion Hello, I own a Centurion that is covered by recall Z-1091-2020 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.
