Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 3 Device Recall UCG Slide Test

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
 Class 3 Device Recall UCG Slide Testsee related information
Date Initiated by FirmFebruary 12, 2010
Date PostedSeptember 25, 2010
Recall Status1 Terminated 3 on May 14, 2012
Recall NumberZ-2500-2010
Recall Event ID 54745
Product Classification Kit, Test, Pregnancy, Hcg, Over The Counter - Product Code LCX
ProductUCG Slide Test; Rapid latex agglutination inhibition slide test for the detection of hCG in urine. Used in the diagnosis of pregnancy.
Code Information Code number 15L3; lot numbers 0115299, Exp. 4.12.2010; 0632299, Exp. 7/30/2010; 0811039, Exp. 10/20/2009; Code number 15L5; lot numbers 0135029, Exp. 3.4.2010; 0221099, Exp. 4/12/2010; 0311179, Exp 5/27/2010; 0634299, Exp. 7/30/2010 and 0814039, Exp. 10/20/2010; Code number 15L8: lot numbers: 0136029, Exp. 3/4/2010; 0220099, Exp. 04/12/2010; 0627299, Exp. 07/30/2010; 0817039, Exp. 10/20/2010.
Recalling Firm/
Manufacturer		 Inverness Medical Professional Diagnostics
2 Research Way
Princeton NJ 08540-6628
For Additional Information ContactInverness Medical Technical Service
877-441-7440
Manufacturer Reason
for Recall		Specific lots no longer meet their stated limit of detection claims of 2000 mIU/mL for the UCG-Slide test and 500 mIU/mL for the UCG-Beta Slide Monoclonal II test.
FDA Determined
Cause 2		Other
ActionThe recall was initiated on February 12, 2010. Letters were sent by Fed Ex on 2/12/2010.
Quantity in Commerce1052 kits
DistributionDistributed Nationwide and to Australia
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
-
-