Use cautionMedical device recall · FDA · Published January 24, 2022
Philips Respironics V60 Plus Ventilator Recall: Expired Adhesive May Cause Silent Shutdown
Philips Respironics recalls V60 Plus Ventilators with part number 1138747 due to expired adhesive that may cause silent shutdowns. Affected units have specific serial numbers listed in the recall notice.
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).
Take action
Contact the company
📍Recalling firmRespironics California, LLC2271 Cosmos Ct · Carlsbad, CA 92011-1517
✎ GovInfoNow plain-language explainer
Philips Respironics is recalling a limited number of V60 Plus Ventilators (part number 1138747) because some units were assembled with expired adhesive. If the adhesive fails, a bracket may become loose and damage capacitors, potentially causing the ventilator to stop providing ventilation without warning (silent shutdown). Read more at govinfonow.com/recall/61225-philips-respironics-v60-plus-ventilator-recall-expired-adhesive-may-cause.
“Philips Respironics V60 Plus Ventilator Recall: Expired Adhesive May Cause Silent Shutdown.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61225-philips-respironics-v60-plus-ventilator-recall-expired-adhesive-may-cause. Based on FDA recall #Z-0663-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0663-2022%22&limit=1).
Respironics California, LLC recalled Philips Respironics V60 Plus Ventilators with part number 1138747 due to a Class I hazard. The Food and Drug Administration announced the recall on Jan. 24, 2022.
How to tell if you have it
Philips Respironics V60 Plus Ventilator, Part Number 1138747
UPC: 00884838090996
Serial Numbers: MX0016240 through MX0018224 (as listed in record)
Sold in AR, CA, FL, GA, IN, LA, MD, MO, NY, PA, SC, TN and TX
The hazard
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.
Context
GovInfoNow's records show Respironics California, LLC has 7 other recalls on record since Sept. 11, 2019. Other recent recalls of similar products include Philips Respironics V60 Plus Ventilator Recall (Feb. 28, 2022), Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10 (June 18, 2021) and Respironics Ventilator Battery Recall (Jan. 6, 2021). Other recent recalls of similar products include Philips Respironics Trilogy EV300 Ventilator Software Update Risk (March 2, 2026), Philips Allura Xper FD10F Medical System Recall (Dec. 15, 2025) and Philips Allura Xper FD10C Medical System Recall (Dec. 15, 2025).
How to tell if you have this one
Check if your ventilator has part number 1138747 and serial numbers listed in the recall notice (MX0016240 through MX0018224). The affected units are limited to specific models and serial numbers.
Brand
Philips Respironics
Product
Philips Respironics V60 Plus Ventilator Part Number 1138747
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class I
Status
Ongoing
Distribution
U.S.: AR, CA, FL, GA, IN, LA, MD, MO, NY, PA, SC, TN and TX. O.U.S. N/A
Recall number
Product, codes & lots
Quantity
Z-0662-2022
Philips Respironics V60 Ventilator Part Number 1053617; The Component of the Ventilators that is impacted is: N 1034132 BRACKET, CAPACITOR,MOTOR DRIVER PCB Model V60 Part Number: 1053617 Serial Numbers/UDI Code: MX0016593 / (01)00884838020054(21)MX0016593 MX0016797 / (01)00884838020054(21)MX0016797 MX0016824 / (01)00884838020054(21)MX0016824 MX0016827 / (01)00884838020054(21)MX0016827 MX0016830 / (01)00884838020054(21)MX0016830 MX0016839 / (01)00884838020054(21)MX0016839 MX0016840 / (01)00884838020054(21)MX0016840 MX0016841 / (01)00884838020054(21)MX0016841 MX0016845 (01)00884838020054(21)MX0016845 MX0016853 (01)00884838020054(21)MX0016853 MX0016867 (01)00884838020054(21)MX0016867 MX0016870 (01)00884838020054(21)MX0016870 MX0016871 (01)00884838020054(21)MX0016871 MX0016872 (01)00884838020054(21)MX0016872 MX0016875 (01)00884838020054(21)MX0016875 MX0016878 (01)00884838020054(21)MX0016878
Verify your ventilator's part number is 1138747 and serial number matches the list of affected units (MX0016240 through MX0018224).
Contact Manufacturer
If your ventilator is affected, contact Philips Respironics for instructions on how to address the issue.
Where it went and when
Where it was distributed
Distributed in 13 states.
Listed by the agency
Not listed
FDA distribution: “U.S.: AR, CA, FL, GA, IN, LA, MD, MO, NY, PA, SC, TN and TX. O.U.S. N/A” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arkansas, California, Florida, Georgia, Indiana, Louisiana, Maryland, Missouri, New York, Pennsylvania, South Carolina, Tennessee, Texas.
Recall timeline
FDA published this recall 44 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0663-2022 (January 24, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0663-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.