Leica Microsystems recalls BOND Ready-To-Use Primary Antibody CDX2 (EP25) REF PA0375 due to potential performance issues. Affected units may not function correctly as per instructions.
Product may not perform as specified in IFU.
Leica Microsystems is recalling a specific antibody product because it might not work properly as described in the user manual. This could affect lab results or experiments if the product doesn't perform as intended.
The product may not function correctly as specified in the user manual. This could lead to inaccurate lab results or failed experiments if the antibody doesn't perform as intended.
Lab researchers and scientists using this antibody product in their work. Those who have the specific product code PA0375 are most at risk.
Check for the product code PA0375 and lot number 69909 on the label. The product is a Ready-To-Use Primary Antibody CDX2 (EP25) from Leica Microsystems.
Look for the product code PA0375 and lot number 69909 on the label to confirm if it's affected.
The recall states the product may not perform as specified in the user manual, but it does not indicate a safety hazard like injury or fire. This is a performance issue, not a safety risk.
The recall does not provide a remedy, so there is no action required beyond checking if you have the affected product.
Check for the product code PA0375 and lot number 69909 on the label. The product is a Ready-To-Use Primary Antibody CDX2 (EP25) from Leica Microsystems.
We’ve drafted a message you can send Leica to request your refund or repair — edit it as you like.
Subject: Recall Z-2481-2021 — Leica Leica Hello, I own a Leica that is covered by recall Z-2481-2021 from Leica. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.