FDA Device recall Z-1152-2020
Respironics V60 Ventilator, Service # 850008, REF: 1053613, 1053614, 1053617, 1053614
- FDA Device
- Class II
- ongoing
- Published 2020-02-19
On 2020-02-19 the FDA classified a Class II recall of Respironics V60 Ventilator, Service # 850008, REF: 1053613, 1053614, 1053617, 1053614 by Respironics California, citing ventilator touchscreen may become frozen and fail to respond to touch commands. If a patient requires a change in therapy, there is no warning associated with an unresponsive touc….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1152-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-09-11 |
| Published | 2020-02-19 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Respironics California |
| Distribution | US |
Product
Respironics V60 Ventilator, Service # 850008, REF: 1053613, 1053614, 1053617, 1053614
Reason
Ventilator touchscreen may become frozen and fail to respond to touch commands. If a patient requires a change in therapy, there is no warning associated with an unresponsive touchscreen, and therefore the clinician would have no prior indication of a touchscreen failure and would be unable to change ventilator settings. The ventilator will continue to function at the predetermined and accepted settings required to support the patient. A delay in therapy adjustments may result in hypercarbia and/or hypoxemia.
Identifiers
| code_info | Serial Numbers: 100005249 100254792 100255723 100255865 100256311 100256502 100256609 100256781 100256875 100257173 10…Serial Numbers: 100005249 100254792 100255723 100255865 100256311 100256502 100256609 100256781 100256875 100257173 100257312 100257583 100257698 100258034 100258360 100258513 100258809 100259082 100259249 100259633 100259878 100260186 100260534 100260846 100261115 100261278 100261538 100261743 100262170 100262417 100262531 100262627 100262821 100007779 100254793 100255724 100255866 100256312 100256503 100256610 100256782 100256876 100257174 100257313 100257584 100257699 100258035 100258361 100258514 100258810 100259083 100259250 100259634 100259879 100260231 100260535 100260847 100261117 100261279 100261539 100261744 100262171 100262418 100262532 100262628 100262822 100007982 100254977 100255725 100255965 100256313 100256504 100256611 100256783 100256877 100257175 100257314 100257585 100257800 100258159 100258362 100258553 100258811 100259085 100259251 100259635 100259880 100260233 100260537 100260849 100261120 100261302 100261540 100261745 100262172 100262419 100262533 100262629 1 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1152-2020%22
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