Urinalysis Test Strips (Macherey Nagel) – Missing Test Pad (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Reagent Test Strips for Blood, Urobilinogen, Bilirubin, Protein, Nitrite, Ketones, Ascorbic Acid, Glucose, pH, Specific Gravity and Leucocytes in Urine by the Dip and Read Technique.
Brand
Macherey Nagel Gmbh & Co. Kg Valencienner Str. 11 Duren Germany
Lot Codes / Batch Numbers
Product #102-2285, UDI/DI: 00304040001479, LOT 65402.
Products Sold
Product #102-2285, UDI/DI: 00304040001479, LOT 65402.
Macherey Nagel Gmbh & Co. Kg Valencienner Str. 11 Duren Germany is recalling Reagent Test Strips for Blood, Urobilinogen, Bilirubin, Protein, Nitrite, Ketones, Ascorbic Acid, Gl due to 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. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
On April4, 2024 URGENT FIELD SAFETY NOTICE letters were sent to direct consignees instructing them to do the following: For distributors: 1. The product named in this safety information must not longer be sold. 2. Confirm the receipt of the information with the attached confirmation of receipt form by April 19, 2024. 3. Pass this safety information on to customers of the affected products. 4. Have the receipt of the information confirmed with the attached confirmation of receipt form. Forward the confirmation forms to our attention using the contact information following. For users: 1. If you have a product Urispec 11-Way, #102-2285, LOT 65402, please check if the leucocytes test pad is present before use of the test strips. 2. Pass the information on to other people and departments who may be working with the product Urispec 11-Way, #102-2285, LOT 65402. 3. Confirm the receipt of the information with the attached confirmation of receipt form by April 19, 2024. 4. If your product is affected, please send the product to your local distributor and arrange for replacement or contact MACHEREY-NAGEL directly. Please make sure in your organization that all users of the above products and other persons to be informed become aware of this Urgent Field Safety Notice. Please keep this information at least until all measures have been completed. Contact persons: Contact for sales / marketing: Dr. Sarah Geenen Product Management Rapid Tests Email: sgeenen@mn-net.com Tel.: +49-(0)2421 969 340, Regulatory contact: Dr. Markus Meusel QAM, Manager Regulatory Affairs Email: mmeusel@mn-net.com Tel. +49 (0) 2421 969 210.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026