FDA Device recall Z-2260-2012
V60 Ventilator, Continuous Ventilator, Model# V60, PN 1056490 Product Usage: The V60 Ventilator is an assist Ventilator and is intended to…
- FDA Device
- Class I
- terminated
- Published 2012-09-12
On 2012-09-12 the FDA classified a Class I recall of V60 Ventilator, Continuous Ventilator, Model# V60, PN 1056490 Product Usage: The V60 Ventilator is an assist Ventilator and is intended to… by Respironics California, citing respironics is recalling the V60 ventilator because certain blower motor assemblies in the V60 ventilators may not meet specifications. Specifically, the impeller may not be prope….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2260-2012 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2012-07-31 |
| Published | 2012-09-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Respironics California |
| Distribution | US |
Product
V60 Ventilator, Continuous Ventilator, Model# V60, PN 1056490 Product Usage: The V60 Ventilator is an assist Ventilator and is intended to augment patient breathing. It is intended for spontaneously breathing individuals who require mechanical ventilation: patients with respiratory failure, respiratory insufficiency, or obstructive sleep apnea in a hospital or other institutional settings under the direction of a physician. The V60 Ventilator is intended to support pediatric patients weighing 20kg (44 Ibs) or greater to adult patients. It is also intended for intubated patients meeting the same selection criteria as the noninvasive applications. It is intended to be used by qualified medical professionals, such as physicians, nurses, and respiratory therapists.
Reason
Respironics is recalling the V60 ventilator because certain blower motor assemblies in the V60 ventilators may not meet specifications. Specifically, the impeller may not be properly seated on the blower motor shaft. This could subsequently cause the blower to cease functioning which would result in the failure of the V60 ventilator to deliver therapy to the patient due to the loss of ventilatio
Identifiers
| code_info | Seria Numbers: 100026615 100029321 100029838 100030462 100030832 100026808 100029324 100029841 100030463 100030833…Seria Numbers: 100026615 100029321 100029838 100030462 100030832 100026808 100029324 100029841 100030463 100030833 100026826 100029325 100029843 100030464 100030834 100027107 100029327 100029845 100030466 100030836 100027181 100029328 100029847 100030468 100030838 100027189 100029330 100030043 100030469 100030840 100027544 100029334 100030106 100030471 100030843 100027660 100029337 100030107 100030472 100030844 100027751 100029455 100030111 100030473 100030845 100027870 100029456 100030112 100030474 100030847 100027872 100029459 100030113 100030475 100030850 100027875 100029462 100030115 100030481 100030977 100028047 100029473 100030117 100030482 100030979 100028053 100029474 100030118 100030485 100030980 100028069 100029500 100030119 100030591 100030983 100028249 100029504 100030120 100030593 100030985 100028324 100029505 100030121 100030594 100030986 100028328 100029507 100030133 100030595 100030987 100028334 100029508 100030204 100030596 100030989 100028339 100 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2260-2012%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.