| Class 2 Device Recall exTEM Assay for the ROTEM delta Thromboelastometry System | |
Date Initiated by Firm | September 13, 2016 |
Create Date | October 23, 2016 |
Recall Status1 |
Terminated 3 on December 05, 2017 |
Recall Number | Z-0302-2017 |
Recall Event ID |
75265 |
510(K)Number | K101533 |
Product Classification |
System, multipurpose for in vitro coagulation studies - Product Code JPA
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Product | ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US, ex-tem.
Used to monitor the coagulation process via the extrinsic pathway in citrated whole blood specimens on the ROTEM delta. |
Code Information |
Lot No. 21929007 |
Recalling Firm/ Manufacturer |
TEM Systems Inc 3210 E Nc Hwy 54 Durham NC 27709
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For Additional Information Contact | Rick Epps 919-941-7777 Ext. 108 |
Manufacturer Reason for Recall | Customers complained of low/empty reagent vials. |
FDA Determined Cause 2 | Nonconforming Material/Component |
Action | Customers were notified of the recall by an Urgent Important Customer Information letter on 9/13/2016. The letter described the device and the problem. Customers were told to stop using the product and to call for replacement product. The letter included a Confirmation of Compliance Letter which was to be completed and returned. |
Quantity in Commerce | 637 boxes x 10 vials |
Distribution | Nationwide Distribution -- AR, CA, DC, GA, HI, ID, IL, IN, LA, ME, MD, MA, MI, MN, MO, NE, NJ, NM, NY, NC, OH, OR, PA, SC, SD, TN, TX, UT, VA, WA, and WV. |
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 = JPA
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