| Date Initiated by Firm | October 26, 2004 |
| Date Posted | April 06, 2005 |
| Recall Status1 |
Terminated 3 on July 22, 2006 |
| Recall Number | Z-0674-05 |
| Recall Event ID |
30924 |
| 510(K)Number | K982879 |
| Product Classification |
System,Test,Antibodies,B2 - Glycoprotein I (B2 - Gpi) - Product Code MSV
|
| Product | Data reduction program written for a specific automated microtiter plate instrument (Bio-Tek ELx800) reader) for use with Diastat Anti-Beta2 Glycoprotein ELISA assay kit. |
| Code Information |
software version 12 |
| FEI Number |
2182595
|
Recalling Firm/ Manufacturer |
Diasorin Inc. 1951 Northwestern Ave S Stillwater MN 55082-7536
|
| For Additional Information Contact | DiaSorin Technical Services 800-328 Ext. 1482 |
Manufacturer Reason for Recall | Data reduction Program written for specific sutomated microtiter plate insturment (Bio-Tek ELx800 reader) is faulty in that the positive result limit is to be greater than 15 U/ml, rather than greater than or equal to 15 U/ml. |
FDA Determined Cause 2 | Other |
| Action | Customers were sent notification letters and effectiveness check form. recommended users manually veify positve results (RSLT), using product insert specifications. |
| Quantity in Commerce | 7 |
| Distribution | CT, MI, MT, UT & CANADA |
| 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 = MSV
|