Date Initiated by Firm | September 29, 2005 |
Date Posted | August 10, 2006 |
Recall Status1 |
Terminated 3 on April 17, 2012 |
Recall Number | Z-1386-06 |
Recall Event ID |
34963 |
510(K)Number | K002290 K980130 K991417 K992859 |
Product Classification |
Blood Gas and Co-Ox Electrolyte & Metabolyte Analyzers - Product Code JFP
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Product | Blood Gas and Co-Ox2 Electrolyte & Metabolyte Analyzers, ABL-700 Series, manufactured from 8/1998 through 11/2004. |
Code Information |
All analyzers manufactured from 8/1998-11/2004, are subject to recall. The devices contain serial numbers 902-441RxxxNxxx. The Rxxx number denotes manufacturing run, and the Nxxx number denotes the individual instrument within the run. |
Recalling Firm/ Manufacturer |
Radiometer America Inc 810 Sharon Dr Westlake OH 44145-1598
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For Additional Information Contact | Vince Sigmund 800-736-0600 |
Manufacturer Reason for Recall | Under certain circumstances, the ABL 700 & 800 Series Blood Gas Analyzers may experience leakage current into the measuring system. Consequently, the analyzers intermittently provide incorrect (too low) result values for Calcium (Ca) and Sodium (Na). |
FDA Determined Cause 2 | Other |
Action | The consignees were notified of this recall by a letter, dated 9/29/2005. The letter informs the customers of this potential problem and the availability of new updated software which will correct the problem. The letter goes on to inform the customer that a Radiometer Service Engineer wil be contacting them shortly in order to arrange for a convenient time to install the software update. Along with the letter, the customer is provided a copy of an additional page and a CD concerning the function and operation of the new software, which is to be added to the customer''s Operator''s Manual. |
Quantity in Commerce | 1615 devices |
Distribution | Nationwide. |
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 = JFP 510(K)s with Product Code = JFP
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