Philips Respironics V60 Ventilator Recall for Backup Battery Failure Risk
Respironics is recalling 934 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a critical life-support device (ventilator) where battery failure poses a risk of harm, but the source text does not report any specific injuries, illnesses, or deaths, fitting the 'High' severity criteria for risk-of-harm products without reported injury.
Plain-English summary
Respironics California, LLC is recalling 934 units of the Philips Respironics V60 Ventilator (Part Number 1053615). The recall is due to a potential issue where the backup battery may fail. This failure can occur if the battery is allowed to over-discharge or if the ventilator is stored for an extended period of time without being plugged into AC power.
The affected devices were distributed worldwide, including nationwide in the United States and in numerous international countries. The ventilators are intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Consumers and healthcare facilities should check their device serial numbers against the list provided in the official recall notice to determine if their unit is affected. If a device is affected, users should contact Respironics for instructions on corrective actions.
The recalled product
- Product
- Philips Respironics V60 Ventilator Part Number 1053615 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
- Manufacturer
- Respironics California, LLC
- Category
- Medical Device — Ventilator
- Affected units
- 934
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Model: V60 Ventilator
- Part Number 1053615 V60 Ventilator
Distribution
Part of a larger recall action
This product is one of 17 recalled by Respironics California, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 17 products in this recall →Related recalls
Same manufacturer · Respironics California, LLC
See all →- SeverePhilips Respironics V680 Ventilator May Stop Operating Due to Electrical Fault
FDA (Devices) · 2022-04-27
- SeverePhilips Respironics V60 Plus Ventilator Recalled for Electrical Circuit Failure Risk
FDA (Devices) · 2022-04-27
- SeverePhilips Respironics V60 Ventilator Recalled Due to Electrical Circuit Defect
FDA (Devices) · 2022-04-27
- SeverePhilips Respironics V60 Plus Ventilators with Defective Adhesive Recalled
FDA (Devices) · 2022-03-09
- SeverePhilips V60 Ventilator Recall: Expired Adhesive May Cause Device Failure
FDA (Devices) · 2022-03-09
Same hazard · battery failure
See all →- HighOdyne Recalls Hybrid Systems Due to Traction Battery Fire Risk
NHTSA · 2026-08-12
- HighHeartMate 3 assist system kits recalled over backup battery failures
FDA (Devices) · 2026-06-24
- HighHeartMate 11 volt lithium ion backup batteries may fail
FDA (Devices) · 2026-06-24
- SevereElgin Pelican Recall: High Voltage Battery Fire Risk
NHTSA · 2026-06-24
- HighHeartMate 3 system controllers recalled over backup battery failures
FDA (Devices) · 2026-06-24