FDA Device recall Z-0901-2021
Philips Respironics V680 Ventilator Part Number 850011 - Product Usage: intended to be used only with various combinations of Respironics-r…
- FDA Device
- Class II
- terminated
- Published 2021-02-03
On 2021-02-03 the FDA classified a Class II recall of Philips Respironics V680 Ventilator Part Number 850011 - Product Usage: intended to be used only with various combinations of Respironics-r… by Respironics California, citing ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended peri….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0901-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-10-30 |
| Published | 2021-02-03 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Respironics California |
| Distribution | US |
Product
Philips Respironics V680 Ventilator Part Number 850011 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Reason
Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
Identifiers
| code_info | Model: V680 Ventilator, Part Number 850011 V60 Ventilator, Finished Serial Numbers: 100138084 100138519 10013852…Model: V680 Ventilator, Part Number 850011 V60 Ventilator, Finished Serial Numbers: 100138084 100138519 100138520 100138521 100138705 100241765 100241766 100241770 100241771 201014177 201014216 201020752 201020756 201020757 201021264 201021272 100260220 100302057 100302058 100305132 100305134 100305349 100306061 100306064 100306070 201025414 201026091 201026102 201026480 201026481 100142436 100183705 201013216 100148515 100220768 100148513 100180915 100220764 201010433 201028445 201028451 100129149 100219325 100220765 100147302 100138085 100138509 100138511 100138517 100147215 100219037 100219322 100219332 201032777 201032778 201032844 100181643 201028444 100191242 100191243 100191244 100191245 100191246 100191247 100191249 100191250 100191251 100191252 100191253 100191254 100191255 100191256 100191257 100191259 100191321 100191325 100191326 100192522 100218827 100220780 201026491 201026492 100125151 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0901-2021%22
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