| Date Initiated by Firm | January 03, 2018 |
| Date Posted | March 20, 2018 |
| Recall Status1 |
Terminated 3 on July 03, 2018 |
| Recall Number | Z-1172-2018 |
| Recall Event ID |
79536 |
| 510(K)Number | K955349 |
| Product Classification |
Patch, pledget and intracardiac, petp, ptfe, polypropylene - Product Code DXZ
|
| Product | HEMASHIELD Knitted Double Velour Cardiovascular Fabric |
| Code Information |
UDI code: 00384401017899 Catalog number: M002000195140 Lot number: 16M21 Serial number: 1092238229 |
| FEI Number |
3012092534
|
Recalling Firm/ Manufacturer |
GETINGE US SALES LLC
45 Barbour Pond Dr
Wayne
NJ
07470-2094
|
| For Additional Information Contact | Josefino Cabinian 973-709-7791 |
Manufacturer Reason for Recall | A probable mislabeling of the product: a different-sized product is referenced on the product packaging label (i.e. 2.5 cm (width) x 7.6 cm (length)) while the actual product inside the box is 2.5 cm (width) x 15 cm (length). |
FDA Determined Cause 2 | Labeling mix-ups |
| Action | On January 3, 2018 an URGENT MEDICAL DEVICE RECALL NOTICE was issued to the (1) affected customer. A return authorization was issued with the recall letter, which is intended to be returned to the recalling firm. Questions or concerns can be directed to 1-800-528-7486 |
| Quantity in Commerce | 1 |
| Distribution | FL |
| 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 = DXZ
|