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 2 Device Recall VIDAS Lyme IgG and IgM (LYT) Assay

  • 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 2 Device Recall VIDAS Lyme IgG and IgM (LYT) Assay see related information
Date Initiated by Firm October 28, 2003
Date Posted July 20, 2004
Recall Status1 Terminated 3 on August 13, 2004
Recall Number Z-0316-04
Recall Event ID 27577
510(K)Number K943812  
Product Classification Reagent, Borrelia Serological Reagent - Product Code LSR
Product VIDAS Lyme IgG and IgM LYT, Ref #30 298, containing 60 LYT STR (reagent strip labels), 2 x 30 LYT SPR (Solid Phase Receptable) pouches, 1 x 1.5 ml LYT C1 (human) (positive control bottle), 1 x 1.5 ml LYT C2 (human) (negative control bottle), and 1 x 1.5 ml LYT S1 (human) (standard bottle). The responsible firm on the kit label is bioMerieux sa, 69280 Marcy l''Etoile France. The responsible firm on the insert is bioMerieux, Inc., Durham, NC.
Code Information Lot #777450001
Recalling Firm/
Manufacturer		 Biomerieux, Inc.
100 Rodolphe St
Durham NC 27712-9402
For Additional Information Contact Anita M. McClernon, MS, RAC
919-620-2288
Manufacturer Reason
for Recall		 Kit may contain incorrect components
FDA Determined
Cause 2		 Other
Action Recall letters dated 10/28/03 were issued via regular mail instructing the customer to examine the kits to determine whether they contain the CMV IgG SPRS and destroy them if found.
Quantity in Commerce 329 kits
Distribution Distribution was made nationwide to hospitals and laboratories.
Total Product Life Cycle TPLC 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.
510(K) Database 510(K)s with Product Code = LSR and Original Applicant = BIOMERIEUX VITEK, INC.
-
-