| Class 2 Device Recall Roche Diagnostics CREP2 | |
Date Initiated by Firm | June 11, 2008 |
Date Posted | October 09, 2008 |
Recall Status1 |
Terminated 3 on September 22, 2009 |
Recall Number | Z-0008-2009 |
Recall Event ID |
48638 |
510(K)Number | K024098 |
Product Classification |
Creatinine Test System - Product Code JFY
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Product | Roche Diagnostics CREP2, Creatinine Plus Ver. 2, COBAS INTEGRA, cobas c systems, Roche Diagnostics, Indianapolis, IN.; 03263991190.
An in-vitro diagnostic reagent system intended for use on COBAS Integra systems for the quantitative determination of creatine in serum, urine and plasma. |
Code Information |
Lot 60064001. |
Recalling Firm/ Manufacturer |
Roche Diagnostics Corp. 9115 Hague Rd Indianapolis IN 46256-1025
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For Additional Information Contact | 800-428-2336 |
Manufacturer Reason for Recall | Some of the labels are glossy, resulting in the bar code being difficult to read by the bar code reader. |
FDA Determined Cause 2 | Labeling Change Control |
Action | Consignees were notified via an Urgent Medical Device correction letter dated 6/11/08 informing users of the problem and providing them with work-around instructions. The instructions suggests 1) inserting the cassette rack slowly; 2) using mainly reagent slots A, B, or C; 3) tilting the rack slightly clockwise so the barcode scanner does not read the barcode at an exact 90 degree angle; and 4) confirming the rack is properly seated on the track and displayed on the Cassette Status screen. If the cassette barcode does not register after following the Work-Around instructions, then customers are required to contact Diagnostics Technical Support. |
Quantity in Commerce | 1068 |
Distribution | Nationwide Distribution |
Total Product Life Cycle | TPLC Device Report |
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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.
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510(K) Database | 510(K)s with Product Code = JFY
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