| Brand Name | DreamStation |
| Common Device Name | Ventilator, Non-Continuous (Respirator) |
| Manufacturer (Section D) |
| Respironics, Inc. |
| 1001 murry ridge lane |
| murrysville PA |
|
| Manufacturer (Section G) |
| Respironics, Inc. |
| 1001 murry ridge lane |
|
| murrysville PA |
|
| Manufacturer Contact |
|
melissa
rosko
|
| 1001 murry ridge lane |
| murrysville, PA
|
|
+1(724)733-0200
|
|
| MDR Report Key | 50528585 |
| Report Number | 2518422-2026-044225 |
| Device Sequence Number | 10163234 |
| Product Code |
BZD
|
| Combination Product (Y/N) | N |
| Initial Reporter Country | CA |
| PMA/510(K) Number | K131982 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Serviced by Third Party (Y/N) | Y |
| Reporter Type |
Manufacturer
|
| Report Source |
Other,Foreign |
| Initial Reporter Occupation |
505
|
| Remedial Action |
Recall |
| Type of Report
| Initial |
| Report Date (Section B) |
08/31/2026 |
| 1 Device was Involved in the Event |
|
| 1 Patient was Involved in the Event |
|
| Is this an Adverse Event Report? |
No
|
| Is this a Product Problem Report? |
Yes
|
| Operator of Device |
Other
|
| Device Model Number | CAX500T12W |
| Device Catalogue Number | CAX500T12W |
| Was Device Available for Evaluation? |
No
|
| Is the Reporter a Health Professional? |
No
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 07/31/2026 |
| Initial Report FDA Received Date | 08/31/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
No
|
| Date Device Manufactured | 09/18/2017 |
| Is the Device Labeled for Single Use? (Y/N) |
No
|
Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N) |
No
|
| Usage of Device |
Reuse
|
If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement | Z-1974-2021 |
| Patient Sequence Number | 1 |
| Patient Sex | Unknown |
|
|