The Recall Desk
HighFDA (Devices)·Z-0891-2021·Announced 2021-02-03

Philips Respironics V60 Ventilator Recall for Backup Battery Failure Risk

Respironics is recalling 3,752 V60 Ventilators worldwide due to a risk of backup battery failure 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 is classified as FDA Class II, and the hazard involves a life-support device (ventilator) where battery failure could lead to harm, but no specific injuries or deaths are reported in the source text.

Plain-English summary

Respironics California, LLC is recalling 3,752 units of the Philips Respironics V60 Ventilator (Part Number 1076709). The recall is due to a potential issue where the backup battery may fail if it is allowed to over-discharge or if the ventilator is stored for an extended period without being plugged into AC power.

The affected devices were distributed worldwide, including in the United States and 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 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 follow the instructions provided by Respironics regarding the recall.

The recalled product

Product
Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Affected units
3,752

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 (4)

  • Model: V60 Ventilator
  • Part Number 1076709 V60 Ventilator
  • JAPAN OPT: CFLEX
  • AVAPS

Distribution

Distributed nationwide across the United States.

The notice also names 54 states specifically:

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 →