Inverness Medical Professional Diagnostics NOW Legionella Urinary Antigen Test. 22 test kit. For In Vitro Diagnostic Use Product Code: 852-000 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
NOW Legionella Urinary Antigen Test. 22 test kit. For In Vitro Diagnostic Use Product Code: 852-000
Brand
Inverness Medical Professional Diagnostics
Lot Codes / Batch Numbers
Lot Number: 024448 Exp. Date: March 14, 2008
Products Sold
Lot Number: 024448 Exp. Date: March 14, 2008
Inverness Medical Professional Diagnostics is recalling NOW Legionella Urinary Antigen Test. 22 test kit. For In Vitro Diagnostic Use Product Code: 852-00 due to Mislabeled product: Outer kit label reads NOW Legionella Urinary Antigen Test, inside contains S. pneumonia test pouches. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Mislabeled product: Outer kit label reads NOW Legionella Urinary Antigen Test, inside contains S. pneumonia test pouches
Recommended Action
Per FDA guidance
Binax Inc. DBA Inverness Medical notified consignees by letter on 09/29/06 advising users to return unused product and distributors to recall to the user level.
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