Centurion recalls specific biopsy trays and latex tubing packs due to incomplete sterile seals that may compromise sterility. Affected products include P151659 Biopsy Tray and P243133 Latex Tubing Packs with lot numbers from 2018110990 to 2019050690.
Incomplete seals on the sterile package may compromise the sterility
Centurion is recalling biopsy trays and latex tubing packs because the sterile packaging may not seal properly, risking contamination. This could lead to infections if the products are used in medical procedures without proper sterility.
Incomplete seals on the sterile packaging could allow contaminants to enter the products, potentially causing infections during medical procedures. This risk is present if the products are used without proper sterility checks.
Medical professionals and patients who use these products during procedures are most at risk. The specific products and lot numbers are listed in the recall notice.
Check for the product names: P151659 Biopsy Tray or P243133 Latex Tubing Packs. Lot numbers range from 2018110990 to 2019050690, with specific dates listed in the recall notice.
Review the lot numbers on the packaging to see if they fall within the range 2018110990 to 2019050690.
The affected products are P151659 Biopsy Tray and P243133 Latex Tubing Packs with lot numbers from 2018110990 to 2019050690.
Look for the product names and lot numbers listed in the recall notice: P151659 Biopsy Tray or P243133 Latex Tubing Packs with lot numbers between 2018110990 and 2019050690.
The recall does not require immediate discontinuation; check the lot numbers to determine if your product is affected.
We’ve drafted a message you can send Centurion to request your refund or repair — edit it as you like.
Subject: Recall Z-1095-2020 — Centurion Centurion Hello, I own a Centurion that is covered by recall Z-1095-2020 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.