| Date Initiated by Firm | January 03, 2005 |
| Date Posted | March 08, 2005 |
| Recall Status1 |
Terminated 3 on September 08, 2005 |
| Recall Number | Z-0571-05 |
| Recall Event ID |
30765 |
| 510(K)Number | K902859 K970839 |
| Product Classification |
Ventilator, Continuous, Facility Use - Product Code CBK
|
| Product | Servo-Ventilator, SV300/300A, Part numbers 6070391 and 6424704. The Safety Alert action targets customers with Unit Serial numbers 24578 and lower. Manuf. Maquet Critial Care AB, SE-171 95 Solna, Sweden. |
| Code Information |
All units with the Serial Numbers 24578 and lower. Total of 7920 units. |
Recalling Firm/ Manufacturer |
Maquet Inc 1140 Route 22 East Bridgewater NJ 08807-2912
|
| For Additional Information Contact | Mr. Jamie Yieh 908-947-2311 |
Manufacturer Reason for Recall | Failures of the air and oxygen gas modules occurred because of misuse/non-compliance of directions. |
FDA Determined Cause 2 | Other |
| Action | Customer letter mailed on January 3, 2005 via certified postage, with return self-addressed postcards that customers must complete to acknowledge receipt of the instructions to refer to their Service and Operating Manuals. |
| Quantity in Commerce | 7920 units |
| Distribution | The ventilators were distributed to hospitals nationwide. There are 33 VA Medical Center and DOD hospitals nationwide. |
| 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 = CBK 510(K)s with Product Code = CBK
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