Date Initiated by Firm | August 14, 2018 |
Create Date | November 12, 2019 |
Recall Status1 |
Terminated 3 on December 20, 2019 |
Recall Number | Z-0362-2020 |
Recall Event ID |
83707 |
510(K)Number | K140078 |
Product Classification |
System, thermal regulating - Product Code DWJ
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Product | TECOTHERM NEO, 100-130/200-240 VAC, 50-60 Hz/ max. 350VA, Class I, Schutzklasse I IP 20, UDI: 04260498580002 - Product Usage: The Thermo-Regulation System TECOTHERM NEO is designed for controlled cold & heat treatment procedures. By means of a mattress, cold and heat is provided to the patient, depending on the therapy objective. |
Code Information |
Serial Numbers: 2018/09/07, 2018/10/01, 2018/10/02, 2018/10/03, 2018/10/05 |
Recalling Firm/ Manufacturer |
Tec Com Gmbh Eingang B Am Krummling 1 Kabelsketal Germany
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Manufacturer Reason for Recall | The action is being initiated due to potential installation of faulty peltier-elements within the thermo-regulation system. Failure of the peltier-element would report a system failure and no longer be able to guarantee temperature control at full power. |
FDA Determined Cause 2 | Nonconforming Material/Component |
Quantity in Commerce | 5 units |
Distribution | US Nationwide distribution in the state of UT. |
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 = DWJ
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