| Date Initiated by Firm | May 08, 2007 |
| Date Posted | September 18, 2007 |
| Recall Status1 |
Terminated 3 on October 29, 2007 |
| Recall Number | Z-1220-2007 |
| Recall Event ID |
38348 |
| 510(K)Number | K000915 |
| Product Classification |
embryo transfer pipettes - Product Code MQK
|
| Product | IVF Pasteur Pipettes, glass, cotton plugged, length 9", in boxes of 90 consisting of 30 nylon tube packages of 3 pipettes each. Item # PP-9-90PL. Boxes are labeled in part ***Humagen Fertility Diagnostics, Inc. 2400 Hunter's Way Charlottesville, VA 22911*** |
| Code Information |
160306022 EXP 1/22/2010 160306046 EXP 2/15/2010 160306065 EXP 3/6/2010 |
Recalling Firm/ Manufacturer |
Humagen Fertility Diagnostics, Inc. 2400 Hunters Way Charlottesville VA 22911-7930
|
| For Additional Information Contact | Cindy Showalter 434-979-4000 |
Manufacturer Reason for Recall | Pasteur pipettes for laboratory use were labeled as sterile but may have become contaminated. |
FDA Determined Cause 2 | Other |
| Action | The recalling firm notified consignees by phone and e-mail on 05/07/07. International consignees were advised to discard product for replacement. |
| Quantity in Commerce | 160 boxes |
| Distribution | The recalled product was distributed to 2 direct accounts in IL and to 6 international distributors in United Kingdom, Greece, Australia, United Arab Emirates, the Netherlands, and Israel. |
| Total Product Life Cycle | TPLC Device Report |
|
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.
|
| 510(K) Database | 510(K)s with Product Code = MQK
|