Medical Device Recalls
-
|
1 to 5 of 5 Results
510(K) Number: K983112 |
|
Results per Page |
|
Product Description
![Sort by Product Name [A-Z]](/scripts/cdrh/images/arrow_up-black.GIF){kind=icon} ![Sort by Product Name [Z-A]](/scripts/cdrh/images/arrow_down-black.GIF){kind=icon}
|
Recall
Class
|
FDA Recall
Posting Date
|
Recalling Firm
|
|---|---|---|---|
| Fisher & Paykel Healthcare RT240 Adult Breathing Circuit Kit. lntended Use: The dual heated ad... | 2 | 12/10/2008 | Fisher & Paykel Healthcare Inc |
| Fisher & Paykel Healthcare Adult Respiratory Ventilator Circuit-Dual Heated Catalogue Number RT211 | 2 | 03/29/2006 | Fisher & Paykel Healthcare Inc |
| Fisher & Paykel Healthcare Adult Respiratory Ventilator Circuit-Dual Heated Catalogue Number RT210 | 2 | 03/29/2006 | Fisher & Paykel Healthcare Inc |
| Fisher & Paykel Healthcare Adult Respiratory Ventilator Circuit-Dual Heated Catalogue Number RT110 | 2 | 03/29/2006 | Fisher & Paykel Healthcare Inc |
| Fisher & Paykel Healthcare Adult Respiratory Ventilator Circuit-Dual Heated Catalogue Number RT111 | 2 | 03/29/2006 | Fisher & Paykel Healthcare Inc |
-
