FDA Device recall Z-1155-2020

Respironics V680 Ventilator, Service # 850011, (OUS Only)

FDA Device
Class II
ongoing
Published 2020-02-19

On 2020-02-19 the FDA classified a Class II recall of Respironics V680 Ventilator, Service # 850011, (OUS Only) 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-1155-2020
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 V680 Ventilator, Service # 850011, (OUS Only)

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 touchcreen, 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: 100255874, 100255957, 100257487, 100257488, 100257490, 100257491, 100257493, 100257494, 100257… Serial Numbers: 100255874, 100255957, 100257487, 100257488, 100257490, 100257491, 100257493, 100257494, 100257495, 100257496, 100257497, 100257498, 100257499, 100257500, 100257501, 100258060, 100258061, 100258063, 100258064, 100258065, 100258066, 100258067, 100258068, 100260220, 100260221, 100260222, 100260223, 100260224, 100260227, 100260228, 100260229, 100260616, 100260617, 100260618, 100260619, 100260620, 100260621, 100260622, 100260623, 100260624, 100260625, 100260626, 100260627, 100260628, 100260629, 100260630, 100260631, 100260632, 100260633, 100260634, 100260635, 100261843, 100261844, 100261845, 100261846, 100261847, 100261848, 100261849, 100261850, 100261851, 100261852, 100261853, 100261854, 100261855, 100261856, 100261857, 100261900, 100261901, 100261902, 100263992, 100263993, 100263994, 100263995, 100263996, 100263997, 100263998, 100263999, 100264020, 100264021, 100264022, 100264023, 100264024,

code_info

Serial Numbers: 100255874, 100255957, 100257487, 100257488, 100257490, 100257491, 100257493, 100257494, 100257…

Serial Numbers: 100255874, 100255957, 100257487, 100257488, 100257490, 100257491, 100257493, 100257494, 100257495, 100257496, 100257497, 100257498, 100257499, 100257500, 100257501, 100258060, 100258061, 100258063, 100258064, 100258065, 100258066, 100258067, 100258068, 100260220, 100260221, 100260222, 100260223, 100260224, 100260227, 100260228, 100260229, 100260616, 100260617, 100260618, 100260619, 100260620, 100260621, 100260622, 100260623, 100260624, 100260625, 100260626, 100260627, 100260628, 100260629, 100260630, 100260631, 100260632, 100260633, 100260634, 100260635, 100261843, 100261844, 100261845, 100261846, 100261847, 100261848, 100261849, 100261850, 100261851, 100261852, 100261853, 100261854, 100261855, 100261856, 100261857, 100261900, 100261901, 100261902, 100263992, 100263993, 100263994, 100263995, 100263996, 100263997, 100263998, 100263999, 100264020, 100264021, 100264022, 100264023, 100264024,

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-1155-2020%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.