# FDA recall Z-0662-2022

> **Respironics California, LLC** · Class I · device recall initiated 2022-01-24.

## Product

Philips Respironics V60 Ventilator Part Number 1053617

## Reason for recall

A limited number of ventilators were assembled with expired adhesive. If the adhesive fails, a bracket may become loose and potentially damage the capacitors, which could cause the ventilator to stop providing ventilation to the patient. This failure may either activate both visual and audible alarms, or it may not sound or display an alarm (a silent shutdown).

## Distribution

U.S.: AR, CA, FL, GA, IN, LA, MD, MO, NY, PA, SC, TN and TX.    O.U.S.  N/A

## Key facts

- **Recall number:** Z-0662-2022
- **Recalling firm:** Respironics California, LLC
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-01-24
- **Report date:** 2022-03-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Carlsbad, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0662-2022

## Citation

> AI Analytics. FDA recall Z-0662-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0662-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*