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U.S. Department of Health and Human Services

Class 2 Device Recall Kit Meter EZCHEM

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  Class 2 Device Recall Kit Meter EZCHEM see related information
Date Initiated by Firm November 02, 2007
Date Posted February 16, 2008
Recall Status1 Terminated 3 on December 09, 2008
Recall Number Z-0724-2008
Recall Event ID 45815
510(K)Number K070068  
Product Classification Ion Based Enzymatic Electrode (Creatinine) - Product Code CGL
Product Nova - EZ CHEM Creatinine Meter: SRS Versions 5.1 and 5.2
P/N 9600, Nova Biomedical, Waltham, MA 02454
Code Information Serial Numbers: 39000207226 39000207229 39000207256 39000207270 39000307226 39000307229 39000307256 39000307270 39000407229 39000407270 39000507226 39000507229 39000507270 39000607229 39000607270 39000707229 39000707270 39000807226 39000807229 39000907270 39001007229 39001007256 39001007270 39001107229 39001107256 39001107270 39001207256 39001207270 39001307256 39001307270 39001407256 39001407270 39001507256 39001507270 39001607256 39001607270 39001707256 39001707270 39001807256 39001807270 39001907256 39001907270 39002007256 39002007270 39002107256 39002107270 39002207256 39002207270 39002307256 39002307270 39002407256 39002407270 39002507256 39002507270 39002607256 39002707256 39002907256 39003007256 39003107256 39003207256 39003307256 39006207249 39006307249 39006407249 39006507249 39006607249 39006607263 39006707249 39006707263 39006807249 39006807263 39006907249 39006907263 39007007263 39007107263 39007207263 39007307249 39007407249 39007507249 39007807249 39007907249 39008007249 39008107249 39008207249 39008307249 39008407249 39008507249 39008607249 39009607263 39009707263 39009807263 39009907263 39010007263 39010507275 39010607275 39010707275 39010807275 39010907275 39011007275 39011107275 39011207275 39011507275 39011607275 39011707275 39011807275 39011907275 39012007275 39012107275 39012307275 39012807275 39012907275 39013007275 39013207275 39013307275 39013407275 39013507275 39013607275 39013707275 39013807275 39013907275 39014107275 39014207275 39014307275 39014407275 39014507275 39014607275 39014707275 39014807275 39014907275 39015007275 39015107275 39015207275 39015307275 
Recalling Firm/
Manufacturer		 Nova Biomedical Corporation
200 Prospect St
Waltham MA 02453
For Additional Information Contact Paul W. MacDonald
781-894-0800 Ext. 211
Manufacturer Reason
for Recall		 Incorrect Results - Creatinine results were lower than the laboratory reference method.
FDA Determined
Cause 2		 Device Design
Action Nova Biomedical issued an Urgent: Medical Device Recall notification letter to consignees dated November 19, 2007. The letter addressed the issues with the product(s) and requested that if users had any remaining stock that it must be returned. The firm also provided a Customer Response form to be returned. Questions concerning this recall will be addressed by Gina Vogelsberg at 1-800-544-4624 or by email at gvogelsberg@ezem.com.
Quantity in Commerce 133 units
Distribution Nationwide Distribution, including the state of NY
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 = CGL and Original Applicant = NOVA BIOMEDICAL CORP.
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