Macherey Nagel recalls specific urine test strips due to potential false negative results for leukocytes, which could miss urinary tract infections. Affected lot 65402.
The reason for the recall is one of the test pads, for the parameter leukocytes, was missing on some of the test strips. The issue was identified by a consumer by way of a Henry Schein Inc. (HSI) customer complaint. This problem can potentially result in the possibility that the parameter leucocytes (a non-specific marker for urinary track infections and an indicator for inflammatory renal processes) is interpreted instrumentally as a false negative. The following HSI item number and lot number were affected: Urispec¿ 11-Way, #102-2285, LOT 65402.
Macherey Nagel is recalling certain urine test strips that may show false negative results for leukocytes, meaning infections could go undetected. This affects specific lot numbers sold through Henry Schein.
The test strips may have missing leukocyte pads, causing the instrument to show false negative results for leukocytes. This could mean urinary tract infections or kidney inflammation go undetected.
Users of urine test strips with the lot number 65402 (item #102-2285) are affected. Most at risk are those who rely on these strips for urinary health monitoring.
Check for the lot number 65402 on the packaging. The product is labeled as Urispec 11-Way, item #102-2285.
Look for the lot number 65402 on the packaging of the Urispec 11-Way test strips.
The recall is due to missing leukocyte pads in some test strips, which can cause false negative results for leukocytes, potentially missing urinary tract infections.
Check the lot number on the packaging; if it's 65402, contact Henry Schein for guidance.
The recall addresses potential false negative results, not physical injury. The risk is low and related to missed health issues.
We’ve drafted a message you can send Machere: 102-2285 to request your refund or repair — edit it as you like.
Subject: Recall Z-1834-2024 — Machere: 102-2285 Machere: 102-2285 Hello, I own a Machere: 102-2285 that is covered by recall Z-1834-2024 from Machere: 102-2285. 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.