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U.S. Department of Health and Human Services

Class 2 Device Recall Roche Ammonia/Ethanol/CO2 Control N

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 Class 2 Device Recall Roche Ammonia/Ethanol/CO2 Control Nsee related information
Date Initiated by FirmNovember 14, 2007
Date PostedDecember 29, 2007
Recall Status1 Terminated 3 on September 22, 2009
Recall NumberZ-0378-2008
Recall Event ID 45805
510(K)NumberK031880 
Product Classification Analyte Calibrator - Product Code JJY
ProductRoche Ammonia/Ethanol/CO2 Control N (Normal) for use in conjunction with Roche/Hitachi, COBAS INTEGRA, cobas c111 and cobas c 501 clinical chemistry analyzers; Catalog. No. 20752401190. Roche Diagnostics Corporation, Indianapolis, IN 46250
Code Information Lot No: 178993-01 and 178993-02; exp. 3/31/2008.  
Recalling Firm/
Manufacturer		 Roche Diagnostics Corp.
9115 Hague Rd
Indianapolis IN 46250-0416
For Additional Information Contact
800-428-2336
Manufacturer Reason
for Recall		High Quality Control Recovery: Undetected high quality control recovery in bicarbonate assay.
FDA Determined
Cause 2		Process design
ActionConsignees were notified of this recall by an Urgent Medical Device Recall letter sent on 11/14/07. The letter instructed the users to immediately discontinue use of Ammonia/ Ethanol/CO2 Control N and Ammonia/Ethanol/CO2 Control A (with listed lots) for quality control assessment of the bicarbonate assay. They were informed that controls may still be used to assess ammonia and ethanol, but alternative controls must be used for assessment of the bicarbonate assay. Consignees are instructed to destroy products at their facility. Consignees were notified of the availability of replacement product via letter dated .
Quantity in Commerce811
DistributionNationwide Distibution
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.
510(K) Database510(K)s with Product Code = JJY
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