Respironics California Inc

Complete recall history across all FDA and CPSC categories — 7 total recalls

Respironics California Inc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (7)

FDA medical device enforcement actions by Respironics California Inc

Date Product Reason Class
Apr 24, 2017 Philips V60 Ventilators, Material No. 850008, 1053613, 1053614, 1053615, 1053... Over time, low-frequency vibrations can cause the pins within the female conn... Class I
Feb 1, 2017 Philips V60 Ventilator with Version 2.20 Software, Description: V 60 Ven... The V60 Ventilator with Version 2.20 software installed may falsely detect th... Class II
Oct 29, 2014 Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit V... If the power supply fan mounting screws are installed incorrectly, the ends o... Class II
Sep 17, 2014 Esprit V1000 and V200 Ventilators, Model No. V1000 and V200; and the 3rd Gene... A failure of a specific component may prevent the ventilators from operating ... Class I
Jun 4, 2013 Respironics V60 Ventilator, Model #V60 Respironics Material P/N (Philips 1... Respironics California, Inc. has initiated a recall on the V60 ventilator bec... Class I
Jul 31, 2012 V60 Ventilator, Continuous Ventilator, Model# V60, PN 1056490 Product Usag... Respironics is recalling the V60 ventilator because certain blower motor asse... Class I
Oct 29, 2007 Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics, Model... The power to the Esprit Display's Backlight is interrupted, causing the GUI t... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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