Date Initiated by Firm | March 26, 2015 |
Date Posted | May 01, 2015 |
Recall Status1 |
Terminated 3 on December 31, 2015 |
Recall Number | Z-1572-2015 |
Recall Event ID |
70841 |
510(K)Number | K970714 |
Product Classification |
Apparatus, autotransfusion - Product Code CAC
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Product | 1/4 in. Curved Trocar with Wound Drain
Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection from the sharp end of the trocar during handling. The double trocar wound drain has metal trocars on either side of the flexible wound drain tube. These are also equipped with trocar guards. |
Code Information |
Part Number:0225-019-000 and lot numbers: 10111012 11018012 11273012 12296012 13066012 13175012 14029012 14143012 10131012 11115012 12237012 |
Recalling Firm/ Manufacturer |
Stryker Instruments Div. of Stryker Corporation 4100 E Milham Ave Portage MI 49002-9704
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For Additional Information Contact | Angela Ragainis 269-323-7700 |
Manufacturer Reason for Recall | Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulating Bulb for a potential sterility breach in the packaging
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FDA Determined Cause 2 | Package design/selection |
Action | An URGENT MEDICAL DEVICE NOTIFICATION letter was sent to all customers on 03/31/2015. The letter identified the affected product, the reason for the recall, the risk to health, and actions to be taken by the customer or user. All are asked to sign the Business Reply Form stating they have read the Notification and followed all instructions within. Customers were asked to immediately check all inventory and quarantine any affected product, return affected product to Stericycle for destruction using a return label provided by Stericycle. Upon receipt of affected product a credit will be issued to customer account. |
Quantity in Commerce | 120 boxes (1200 each) |
Distribution | Worldwide Distribution. US nationwide, Australia, Great Britain, The Netherlands, Spain, Romania, Greece, Switzerland, South Africa, and Japan. |
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 = CAC
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