Date Initiated by Firm | August 07, 2015 |
Date Posted | August 19, 2015 |
Recall Status1 |
Terminated 3 on March 01, 2016 |
Recall Number | Z-2422-2015 |
Recall Event ID |
71911 |
510(K)Number | K963756 |
Product Classification |
Sucker, cardiotomy return, cardiopulmonary bypass - Product Code DTS
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Product | IBC Suction Wand Catalog Number 1990S
Product Usage:
The IBC Suction Wand is a component of Blood Recovery System for use in open heart procedures, autologous blood recovery and blood suction. It is a disposable, single use component. |
Code Information |
033115-3445 |
Recalling Firm/ Manufacturer |
International Biophysics Corp. Bldg 2, Ste 275 2101 E Saint Elmo Rd Austin TX 78744-1015
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For Additional Information Contact | Geoff Marcek 512-814-0046 |
Manufacturer Reason for Recall | It was discovered that the heat seal placed onto sterile pouches may not meet strength acceptance criteria. |
FDA Determined Cause 2 | Packaging process control |
Action | The recalling firm began notifying their affacted customers on 7/2/2015 |
Quantity in Commerce | 100 units |
Distribution | Worldwide - United States Nationwide and the countries of: Germany, Norway, Turkey, Chile, Pakistan, and Republic of South Africa |
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 = DTS
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